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rs397508065

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508065(G;T)
Make rs397508065(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319106
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508065
ebirs397508065
HLIrs397508065
Exacrs397508065
Varsomers397508065
Maprs397508065
PheGenIrs397508065
hapmaprs397508065
1000 genomesrs397508065
hgdprs397508065
ensemblrs397508065
gopubmedrs397508065
geneviewrs397508065
scholarrs397508065
googlers397508065
pharmgkbrs397508065
gwascentralrs397508065
openSNPrs397508065
23andMers397508065
23andMe allrs397508065
SNP Nexus

SNPshotrs397508065
SNPdbers397508065
MSV3drs397508065
GWAS Ctlgrs397508065
Max Magnitude0
ClinVar
Risk rs397508065(T;T)
Alt rs397508065(T;T)
Reference rs397508065(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893243G>T
CLNSRC ClinVar
CLNACC RCV000045898.2,