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rs397508060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397508060(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332430
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508060
ClinGenrs397508060
ebirs397508060
HLIrs397508060
Exacrs397508060
Varsomers397508060
Maprs397508060
PheGenIrs397508060
hapmaprs397508060
1000 genomesrs397508060
hgdprs397508060
ensemblrs397508060
gopubmedrs397508060
geneviewrs397508060
scholarrs397508060
googlers397508060
pharmgkbrs397508060
gwascentralrs397508060
openSNPrs397508060
23andMers397508060
23andMe allrs397508060
SNP Nexus

SNPshotrs397508060
SNPdbers397508060
MSV3drs397508060
GWAS Ctlgrs397508060
Max Magnitude6
ClinVar
Risk rs397508060(T;T)
Alt rs397508060(T;T)
Reference Rs397508060(A;A)
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.32906567A>T
CLNSRC ClinVar
CLNACC RCV000045849.2, RCV000241210.2,