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rs397508040

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508040(-;-)
Make rs397508040(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380116
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508040
ebirs397508040
HLIrs397508040
Exacrs397508040
Varsomers397508040
Maprs397508040
PheGenIrs397508040
hapmaprs397508040
1000 genomesrs397508040
hgdprs397508040
ensemblrs397508040
gopubmedrs397508040
geneviewrs397508040
scholarrs397508040
googlers397508040
pharmgkbrs397508040
gwascentralrs397508040
openSNPrs397508040
23andMers397508040
23andMe allrs397508040
SNP Nexus

SNPshotrs397508040
SNPdbers397508040
MSV3drs397508040
GWAS Ctlgrs397508040
Max Magnitude0
ClinVar
Risk rs397508040(;)
Alt rs397508040(;)
Reference rs397508040(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.32954253delG
CLNSRC ClinVar
CLNACC RCV000045752.2,