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rs397507938

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507938(C;C)
Make rs397507938(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357929
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507938
ebirs397507938
HLIrs397507938
Exacrs397507938
Varsomers397507938
Maprs397507938
PheGenIrs397507938
hapmaprs397507938
1000 genomesrs397507938
hgdprs397507938
ensemblrs397507938
gopubmedrs397507938
geneviewrs397507938
scholarrs397507938
googlers397507938
pharmgkbrs397507938
gwascentralrs397507938
openSNPrs397507938
23andMers397507938
23andMe allrs397507938
SNP Nexus

SNPshotrs397507938
SNPdbers397507938
MSV3drs397507938
GWAS Ctlgrs397507938
Max Magnitude0
ClinVar
Risk rs397507938(C;C)
Alt rs397507938(C;C)
Reference rs397507938(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.32932066G>C
CLNSRC ClinVar
CLNACC RCV000045318.2,