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rs397507845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507845(C;G)
Make rs397507845(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340714
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507845
ebirs397507845
HLIrs397507845
Exacrs397507845
Varsomers397507845
Maprs397507845
PheGenIrs397507845
hapmaprs397507845
1000 genomesrs397507845
hgdprs397507845
ensemblrs397507845
gopubmedrs397507845
geneviewrs397507845
scholarrs397507845
googlers397507845
pharmgkbrs397507845
gwascentralrs397507845
openSNPrs397507845
23andMers397507845
23andMe allrs397507845
SNP Nexus

SNPshotrs397507845
SNPdbers397507845
MSV3drs397507845
GWAS Ctlgrs397507845
Max Magnitude0
ClinVar
Risk rs397507845(G;G)
Alt rs397507845(G;G)
Reference rs397507845(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914851C>G
CLNSRC ClinVar
CLNACC RCV000044923.2,