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rs397507832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507832(C;G)
Make rs397507832(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326599
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507832
ebirs397507832
HLIrs397507832
Exacrs397507832
Varsomers397507832
Maprs397507832
PheGenIrs397507832
hapmaprs397507832
1000 genomesrs397507832
hgdprs397507832
ensemblrs397507832
gopubmedrs397507832
geneviewrs397507832
scholarrs397507832
googlers397507832
pharmgkbrs397507832
gwascentralrs397507832
openSNPrs397507832
23andMers397507832
23andMe allrs397507832
SNP Nexus

SNPshotrs397507832
SNPdbers397507832
MSV3drs397507832
GWAS Ctlgrs397507832
Max Magnitude0
ClinVar
Risk rs397507832(G;G)
Alt rs397507832(G;G)
Reference rs397507832(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.32900736C>G
CLNSRC ClinVar
CLNACC RCV000044862.2,