Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507874(-;-)
Make rs397507874(-;G)
Make rs397507874(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341007
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507874
ebirs397507874
HLIrs397507874
Exacrs397507874
Varsomers397507874
Maprs397507874
PheGenIrs397507874
hapmaprs397507874
1000 genomesrs397507874
hgdprs397507874
ensemblrs397507874
gopubmedrs397507874
geneviewrs397507874
scholarrs397507874
googlers397507874
pharmgkbrs397507874
gwascentralrs397507874
openSNPrs397507874
23andMers397507874
23andMe allrs397507874
SNP Nexus

SNPshotrs397507874
SNPdbers397507874
MSV3drs397507874
GWAS Ctlgrs397507874
Max Magnitude0
ClinVar
Risk rs397507874(G;G)
Alt rs397507874(G;G)
Reference rs397507874(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32915144dupG
CLNSRC ClinVar
CLNACC RCV000045009.2,