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rs397508042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508042(-;-)
Make rs397508042(-;G)
Make rs397508042(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394694
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508042
ebirs397508042
HLIrs397508042
Exacrs397508042
Varsomers397508042
Maprs397508042
PheGenIrs397508042
hapmaprs397508042
1000 genomesrs397508042
hgdprs397508042
ensemblrs397508042
gopubmedrs397508042
geneviewrs397508042
scholarrs397508042
googlers397508042
pharmgkbrs397508042
gwascentralrs397508042
openSNPrs397508042
23andMers397508042
23andMe allrs397508042
SNP Nexus

SNPshotrs397508042
SNPdbers397508042
MSV3drs397508042
GWAS Ctlgrs397508042
Max Magnitude0
ClinVar
Risk rs397508042(G;G)
Alt rs397508042(G;G)
Reference rs397508042(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32968831dupG
CLNSRC ClinVar
CLNACC RCV000045769.2,