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rs397507965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507965(A;A)
Make rs397507965(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363377
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507965
ebirs397507965
HLIrs397507965
Exacrs397507965
Varsomers397507965
Maprs397507965
PheGenIrs397507965
hapmaprs397507965
1000 genomesrs397507965
hgdprs397507965
ensemblrs397507965
gopubmedrs397507965
geneviewrs397507965
scholarrs397507965
googlers397507965
pharmgkbrs397507965
gwascentralrs397507965
openSNPrs397507965
23andMers397507965
23andMe allrs397507965
SNP Nexus

SNPshotrs397507965
SNPdbers397507965
MSV3drs397507965
GWAS Ctlgrs397507965
Max Magnitude0
ClinVar
Risk rs397507965(A;A)
Alt rs397507965(A;A)
Reference rs397507965(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937514G>A
CLNSRC ClinVar
CLNACC RCV000045441.2,