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rs397507662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507662(C;T)
Make rs397507662(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337638
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507662
ebirs397507662
HLIrs397507662
Exacrs397507662
Varsomers397507662
Maprs397507662
PheGenIrs397507662
hapmaprs397507662
1000 genomesrs397507662
hgdprs397507662
ensemblrs397507662
gopubmedrs397507662
geneviewrs397507662
scholarrs397507662
googlers397507662
pharmgkbrs397507662
gwascentralrs397507662
openSNPrs397507662
23andMers397507662
23andMe allrs397507662
SNP Nexus

SNPshotrs397507662
SNPdbers397507662
MSV3drs397507662
GWAS Ctlgrs397507662
Max Magnitude0
ClinVar
Risk rs397507662(T;T)
Alt rs397507662(T;T)
Reference rs397507662(C;C)
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.32911775C>T
CLNSRC ClinVar
CLNACC RCV000044170.2, RCV000162053.1,