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rs276174897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;GAATTT) 6 BRCA2 variant considered pathogenic for breast cancer
(GAATTT;GAATTT) 0 common in clinvar


Make rs276174897(AG;AG)
ReferenceGRCh38 38.1/142
Chromosome13
Position32362638
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174897
ebirs276174897
HLIrs276174897
Exacrs276174897
Varsomers276174897
Maprs276174897
PheGenIrs276174897
hapmaprs276174897
1000 genomesrs276174897
hgdprs276174897
ensemblrs276174897
gopubmedrs276174897
geneviewrs276174897
scholarrs276174897
googlers276174897
pharmgkbrs276174897
gwascentralrs276174897
openSNPrs276174897
23andMers276174897
23andMe allrs276174897
SNP Nexus

SNPshotrs276174897
SNPdbers276174897
MSV3drs276174897
GWAS Ctlgrs276174897
Max Magnitude6
rs276174897, also known as 8149del6insAG, c.7921_7926delinsAG and p.Glu2641_Phe2642?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174897(AG;AG)
Alt rs276174897(AG;AG)
Reference rs276174897(GAATTT;GAATTT)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32936775_32936780delGAATTTinsAG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113839.1,