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rs397508061

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508061(-;-)
Make rs397508061(-;G)
Make rs397508061(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32396933
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508061
ebirs397508061
HLIrs397508061
Exacrs397508061
Varsomers397508061
Maprs397508061
PheGenIrs397508061
hapmaprs397508061
1000 genomesrs397508061
hgdprs397508061
ensemblrs397508061
gopubmedrs397508061
geneviewrs397508061
scholarrs397508061
googlers397508061
pharmgkbrs397508061
gwascentralrs397508061
openSNPrs397508061
23andMers397508061
23andMe allrs397508061
SNP Nexus

SNPshotrs397508061
SNPdbers397508061
MSV3drs397508061
GWAS Ctlgrs397508061
Max Magnitude0
ClinVar
Risk rs397508061(G;G)
Alt rs397508061(G;G)
Reference rs397508061(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32971070dupG
CLNSRC ClinVar
CLNACC RCV000045850.2,