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rs397508063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508063(A;A)
Make rs397508063(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32396968
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508063
ebirs397508063
HLIrs397508063
Exacrs397508063
Varsomers397508063
Maprs397508063
PheGenIrs397508063
hapmaprs397508063
1000 genomesrs397508063
hgdprs397508063
ensemblrs397508063
gopubmedrs397508063
geneviewrs397508063
scholarrs397508063
googlers397508063
pharmgkbrs397508063
gwascentralrs397508063
openSNPrs397508063
23andMers397508063
23andMe allrs397508063
SNP Nexus

SNPshotrs397508063
SNPdbers397508063
MSV3drs397508063
GWAS Ctlgrs397508063
Max Magnitude0
ClinVar
Risk rs397508063(A,T;A,T)
Alt rs397508063(A,T;A,T)
Reference rs397508063(G;G)
Significance Untested
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32971105G>A; NC_000013.10:g.32971105G>T
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000045858.2, RCV000130020.2,