chr1:67694202:A>G Detail (hg19) (IL23R, C1orf141)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:67,694,202-67,694,202 |
| hg38 | chr1:67,228,519-67,228,519 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_001276351.1:c.-104+3327T>C | |
| Ensemble | ENST00000371007.6:c.-104+3327T>C |
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_144701.2:c.956-8194A>G | |
| Ensemble | ENST00000697163.1:c.956-8194A>G | |
| ENST00000697230.1:c.955+8789A>G |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.697 | |
| 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 | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.371 | Crohn Disease | Genome-wide association study for Crohn's disease in the Quebec Founder Populati... | GWASCAT | 17804789 | Detail |
| 0.368 | Crohn Disease | To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... | BeFree | 20066736 | Detail |
| 0.371 | Crohn Disease | To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... | BeFree | 20066736 | Detail |
| 0.560 | Crohn Disease | To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... | BeFree | 20066736 | Detail |
| 0.050 | Crohn Disease | To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and... | BeFree | 20066736 | Detail |
| 0.327 | ulcerative colitis | Genome-wide association identifies multiple ulcerative colitis susceptibility lo... | GWASCAT | 20228799 | Detail |
| 0.311 | psoriasis | Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathw... | GWASCAT | 19169254 | Detail |
| 0.020 | ulcerative colitis | The IL23R rs2201841 homozygous genotype and IBD5 carrier status together did not... | BeFree | 24415875 | Detail |
| 0.327 | ulcerative colitis | The IL23R rs2201841 homozygous genotype and IBD5 carrier status together did not... | BeFree | 24415875 | Detail |
| 0.016 | Arthritis, Psoriatic | IL-23R gene polymorphism rs2201841 is associated with psoriatic arthritis. | BeFree | 24910145 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multip... | DisGeNET | Detail |
| To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... | DisGeNET | Detail |
| To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... | DisGeNET | Detail |
| To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... | DisGeNET | Detail |
| To investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autopha... | DisGeNET | Detail |
| Genome-wide association identifies multiple ulcerative colitis susceptibility loci. | DisGeNET | Detail |
| Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. | DisGeNET | Detail |
| The IL23R rs2201841 homozygous genotype and IBD5 carrier status together did not confer susceptibili... | DisGeNET | Detail |
| The IL23R rs2201841 homozygous genotype and IBD5 carrier status together did not confer susceptibili... | DisGeNET | Detail |
| IL-23R gene polymorphism rs2201841 is associated with psoriatic arthritis. | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs2201841 dbSNP
- Genome
- hg19
- Position
- chr1:67,694,202-67,694,202
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
- 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))
- rs2201841
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.6968
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 11678
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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