chr11:132230702:T>C Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:132,230,702-132,230,702
hg38 chr11:132,360,808-132,360,808 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:0.317
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
<0.001 breast carcinoma In conclusion, the current meta-analysis supports that the miR-196a-2 rs11614913... BeFree 23982873 Detail
<0.001 Malignant neoplasm of breast In conclusion, the current meta-analysis supports that the miR-196a-2 rs11614913... BeFree 23982873 Detail
Annotation

Annotations

DescrptionSourceLinks
In conclusion, the current meta-analysis supports that the miR-196a-2 rs11614913*T, miR-499 rs374644... DisGeNET Detail
In conclusion, the current meta-analysis supports that the miR-196a-2 rs11614913*T, miR-499 rs374644... DisGeNET Detail
Gene
-
dbSNP
rs895919 dbSNP
Genome
hg19
Position
chr11:132,230,702-132,230,702
Variant Type
snv
Reference Allele
T
Alternative Allele
C
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))
rs895919
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.3174
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
5319
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
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