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rs397507931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507931(-;-)
Make rs397507931(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357804
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507931
ebirs397507931
HLIrs397507931
Exacrs397507931
Varsomers397507931
Maprs397507931
PheGenIrs397507931
hapmaprs397507931
1000 genomesrs397507931
hgdprs397507931
ensemblrs397507931
gopubmedrs397507931
geneviewrs397507931
scholarrs397507931
googlers397507931
pharmgkbrs397507931
gwascentralrs397507931
openSNPrs397507931
23andMers397507931
23andMe allrs397507931
SNP Nexus

SNPshotrs397507931
SNPdbers397507931
MSV3drs397507931
GWAS Ctlgrs397507931
Max Magnitude0
ClinVar
Risk rs397507931(;)
Alt rs397507931(;)
Reference rs397507931(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931941delT
CLNSRC ClinVar
CLNACC RCV000045284.2,