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

rs397507340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507340(A;A)
Make rs397507340(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326241
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507340
ebirs397507340
HLIrs397507340
Exacrs397507340
Varsomers397507340
Maprs397507340
PheGenIrs397507340
hapmaprs397507340
1000 genomesrs397507340
hgdprs397507340
ensemblrs397507340
gopubmedrs397507340
geneviewrs397507340
scholarrs397507340
googlers397507340
pharmgkbrs397507340
gwascentralrs397507340
openSNPrs397507340
23andMers397507340
23andMe allrs397507340
SNP Nexus

SNPshotrs397507340
SNPdbers397507340
MSV3drs397507340
GWAS Ctlgrs397507340
Max Magnitude0
ClinVar
Risk rs397507340(A;A)
Alt rs397507340(A;A)
Reference rs397507340(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900378G>A
CLNSRC ClinVar
CLNACC RCV000031503.3, RCV000044487.2,