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rs397507948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507948(C;G)
Make rs397507948(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363172
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507948
ebirs397507948
HLIrs397507948
Exacrs397507948
Varsomers397507948
Maprs397507948
PheGenIrs397507948
hapmaprs397507948
1000 genomesrs397507948
hgdprs397507948
ensemblrs397507948
gopubmedrs397507948
geneviewrs397507948
scholarrs397507948
googlers397507948
pharmgkbrs397507948
gwascentralrs397507948
openSNPrs397507948
23andMers397507948
23andMe allrs397507948
SNP Nexus

SNPshotrs397507948
SNPdbers397507948
MSV3drs397507948
GWAS Ctlgrs397507948
Max Magnitude0
ClinVar
Risk rs397507948(G;G)
Alt rs397507948(G;G)
Reference rs397507948(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937309C>G
CLNSRC ClinVar
CLNACC RCV000045370.2,