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rs276174907

From SNPedia

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Stabilizedplus
Geno Mag Summary
(AA;TAG) 6 BRCA2 variant considered pathogenic for breast cancer
(TAG;TAG) 0 common in clinvar


Make rs276174907(AA;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370464
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174907
ebirs276174907
HLIrs276174907
Exacrs276174907
Varsomers276174907
Maprs276174907
PheGenIrs276174907
hapmaprs276174907
1000 genomesrs276174907
hgdprs276174907
ensemblrs276174907
gopubmedrs276174907
geneviewrs276174907
scholarrs276174907
googlers276174907
pharmgkbrs276174907
gwascentralrs276174907
openSNPrs276174907
23andMers276174907
23andMe allrs276174907
SNP Nexus

SNPshotrs276174907
SNPdbers276174907
MSV3drs276174907
GWAS Ctlgrs276174907
Max Magnitude6
rs276174907, also known as 8622delTAGinsAA, c.8394_8396delTAGinsAA and p.Pro2798_Arg2799ProAsnfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174907(AA;AA)
Alt rs276174907(AA;AA)
Reference rs276174907(TAG;TAG)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32944601_32944603delTAGinsAA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045504.3, RCV000113924.1,