Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507997

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507997(A;A)
Make rs397507997(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371101
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507997
ebirs397507997
HLIrs397507997
Exacrs397507997
Varsomers397507997
Maprs397507997
PheGenIrs397507997
hapmaprs397507997
1000 genomesrs397507997
hgdprs397507997
ensemblrs397507997
gopubmedrs397507997
geneviewrs397507997
scholarrs397507997
googlers397507997
pharmgkbrs397507997
gwascentralrs397507997
openSNPrs397507997
23andMers397507997
23andMe allrs397507997
SNP Nexus

SNPshotrs397507997
SNPdbers397507997
MSV3drs397507997
GWAS Ctlgrs397507997
Max Magnitude0
ClinVar
Risk rs397507997(A,T;A,T)
Alt rs397507997(A,T;A,T)
Reference rs397507997(G;G)
Significance Probable-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.32945238G>A; NC_000013.10:g.32945238G>T
CLNSRC ClinVar
CLNACC RCV000045577.2, RCV000238926.1, RCV000082991.2,