chr18:12779947:G>T Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr18:12,779,947-12,779,947 |
| hg38 | chr18:12,779,948-12,779,948 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.894 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.234 | ulcerative colitis | The study indicates that IL23R-rs11805303 and PTPN2-rs2542151 might contribute t... | BeFree | 22426692 | Detail |
| 0.327 | ulcerative colitis | The study indicates that IL23R-rs11805303 and PTPN2-rs2542151 might contribute t... | BeFree | 22426692 | Detail |
| 0.129 | ulcerative colitis | The study indicates that IL23R-rs11805303 and PTPN2-rs2542151 might contribute t... | BeFree | 22426692 | Detail |
| 0.033 | ulcerative colitis | Epistasis analysis showed weak epistasis between the ATG16L1 SNP rs2241879 and P... | BeFree | 22457781 | Detail |
| 0.003 | ankylosing spondylitis | Polymorphisms associated in the allele frequencies test with severe BASFI/t in a... | BeFree | 22984424 | Detail |
| <0.001 | ankylosing spondylitis | Polymorphisms associated in the allele frequencies test with severe BASFI/t in a... | BeFree | 22984424 | Detail |
| 0.007 | Crohn Disease | [Genome-wide association study of 14,000 cases of seven common diseases and 3,00... | GAD | 17554300 | Detail |
| 0.007 | Diabetes Mellitus, Insulin-Dependent | [Meta-analysis of genome-wide association study data identifies additional type ... | GAD | 18978792 | Detail |
| 0.137 | Diabetes Mellitus, Insulin-Dependent | [Robust associations of four new chromosome regions from genome-wide analyses of... | GAD | 17554260 | Detail |
| 0.137 | Diabetes Mellitus, Insulin-Dependent | [Meta-analysis of genome-wide association study data identifies additional type ... | GAD | 18978792 | Detail |
| 0.129 | ulcerative colitis | The single nucleotide polymorphism (SNP) rs2542151 within the gene locus region ... | BeFree | 22021207 | Detail |
| 0.007 | Crohn Disease | [Sequence variants in the autophagy gene IRGM and multiple other replicating loc... | GAD | 17554261 | Detail |
| 0.248 | rheumatoid arthritis | The single nucleotide polymorphism (SNP) rs2542151 within the gene locus region ... | BeFree | 22021207 | Detail |
| 0.137 | Diabetes Mellitus, Insulin-Dependent | The single nucleotide polymorphism (SNP) rs2542151 within the gene locus region ... | BeFree | 22021207 | Detail |
| 0.007 | Diabetes Mellitus, Insulin-Dependent | [Robust associations of four new chromosome regions from genome-wide analyses of... | GAD | 17554260 | Detail |
| 0.124 | Inflammatory Bowel Diseases | Genomic DNA from 2131 individuals of Caucasian origin (905 patients with CD, 318... | BeFree | 22457781 | Detail |
| 0.007 | Crohn Disease | [Genome-wide association defines more than 30 distinct susceptibility loci for C... | GAD | 18587394 | Detail |
| 0.007 | Diabetes Mellitus, Insulin-Dependent | [Genome-wide association analysis of autoantibody positivity in type 1 diabetes ... | GAD | 21829393 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The study indicates that IL23R-rs11805303 and PTPN2-rs2542151 might contribute to the development of... | DisGeNET | Detail |
| The study indicates that IL23R-rs11805303 and PTPN2-rs2542151 might contribute to the development of... | DisGeNET | Detail |
| The study indicates that IL23R-rs11805303 and PTPN2-rs2542151 might contribute to the development of... | DisGeNET | Detail |
| Epistasis analysis showed weak epistasis between the ATG16L1 SNP rs2241879 and PTPN2 SNP rs2542151 (... | DisGeNET | Detail |
| Polymorphisms associated in the allele frequencies test with severe BASFI/t in all classifications w... | DisGeNET | Detail |
| Polymorphisms associated in the allele frequencies test with severe BASFI/t in all classifications w... | DisGeNET | Detail |
| [Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.] | DisGeNET | Detail |
| [Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci... | DisGeNET | Detail |
| [Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.] | DisGeNET | Detail |
| [Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci... | DisGeNET | Detail |
| The single nucleotide polymorphism (SNP) rs2542151 within the gene locus region encoding protein tyr... | DisGeNET | Detail |
| [Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Croh... | DisGeNET | Detail |
| The single nucleotide polymorphism (SNP) rs2542151 within the gene locus region encoding protein tyr... | DisGeNET | Detail |
| The single nucleotide polymorphism (SNP) rs2542151 within the gene locus region encoding protein tyr... | DisGeNET | Detail |
| [Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.] | DisGeNET | Detail |
| Genomic DNA from 2131 individuals of Caucasian origin (905 patients with CD, 318 patients with UC, a... | DisGeNET | Detail |
| [Genome-wide association defines more than 30 distinct susceptibility loci for Crohn\'s disease.] | DisGeNET | Detail |
| [Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.] | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs2542151 dbSNP
- Genome
- hg19
- Position
- chr18:12,779,947-12,779,947
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs2542151
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.8937
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 14979
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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