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rs397507887

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507887(-;-)
Make rs397507887(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341197
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507887
ebirs397507887
HLIrs397507887
Exacrs397507887
Varsomers397507887
Maprs397507887
PheGenIrs397507887
hapmaprs397507887
1000 genomesrs397507887
hgdprs397507887
ensemblrs397507887
gopubmedrs397507887
geneviewrs397507887
scholarrs397507887
googlers397507887
pharmgkbrs397507887
gwascentralrs397507887
openSNPrs397507887
23andMers397507887
23andMe allrs397507887
SNP Nexus

SNPshotrs397507887
SNPdbers397507887
MSV3drs397507887
GWAS Ctlgrs397507887
Max Magnitude0
ClinVar
Risk rs397507887(;)
Alt rs397507887(;)
Reference rs397507887(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.32915334delG
CLNSRC ClinVar
CLNACC RCV000045069.2,