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rs397507812

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507812(-;-)
Make rs397507812(-;G)
Make rs397507812(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340300
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507812
ebirs397507812
HLIrs397507812
Exacrs397507812
Varsomers397507812
Maprs397507812
PheGenIrs397507812
hapmaprs397507812
1000 genomesrs397507812
hgdprs397507812
ensemblrs397507812
gopubmedrs397507812
geneviewrs397507812
scholarrs397507812
googlers397507812
pharmgkbrs397507812
gwascentralrs397507812
openSNPrs397507812
23andMers397507812
23andMe allrs397507812
SNP Nexus

SNPshotrs397507812
SNPdbers397507812
MSV3drs397507812
GWAS Ctlgrs397507812
Max Magnitude0
ClinVar
Risk rs397507812(G;G)
Alt rs397507812(G;G)
Reference rs397507812(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914437dupG
CLNSRC ClinVar
CLNACC RCV000044797.2,