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rs397507588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507588(-;-)
Make rs397507588(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332922
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507588
ebirs397507588
HLIrs397507588
Exacrs397507588
Varsomers397507588
Maprs397507588
PheGenIrs397507588
hapmaprs397507588
1000 genomesrs397507588
hgdprs397507588
ensemblrs397507588
gopubmedrs397507588
geneviewrs397507588
scholarrs397507588
googlers397507588
pharmgkbrs397507588
gwascentralrs397507588
openSNPrs397507588
23andMers397507588
23andMe allrs397507588
SNP Nexus

SNPshotrs397507588
SNPdbers397507588
MSV3drs397507588
GWAS Ctlgrs397507588
Max Magnitude0
ClinVar
Risk rs397507588(;)
Alt rs397507588(;)
Reference rs397507588(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.32907059delC
CLNSRC ClinVar
CLNACC RCV000043806.2,