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rs276174925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs276174925(C;T)
Make rs276174925(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394898
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174925
ebirs276174925
HLIrs276174925
Exacrs276174925
Varsomers276174925
Maprs276174925
PheGenIrs276174925
hapmaprs276174925
1000 genomesrs276174925
hgdprs276174925
ensemblrs276174925
gopubmedrs276174925
geneviewrs276174925
scholarrs276174925
googlers276174925
pharmgkbrs276174925
gwascentralrs276174925
openSNPrs276174925
23andMers276174925
23andMe allrs276174925
SNP Nexus

SNPshotrs276174925
SNPdbers276174925
MSV3drs276174925
GWAS Ctlgrs276174925
Max Magnitude0
ClinVar
Risk rs276174925(T;T)
Alt rs276174925(T;T)
Reference rs276174925(C;C)
Significance Untested
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.32969035C>T
CLNSRC ClinVar
CLNACC RCV000045828.2, RCV000114113.1,