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rs397507637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507637(-;-)
Make rs397507637(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337056
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507637
ebirs397507637
HLIrs397507637
Exacrs397507637
Varsomers397507637
Maprs397507637
PheGenIrs397507637
hapmaprs397507637
1000 genomesrs397507637
hgdprs397507637
ensemblrs397507637
gopubmedrs397507637
geneviewrs397507637
scholarrs397507637
googlers397507637
pharmgkbrs397507637
gwascentralrs397507637
openSNPrs397507637
23andMers397507637
23andMe allrs397507637
SNP Nexus

SNPshotrs397507637
SNPdbers397507637
MSV3drs397507637
GWAS Ctlgrs397507637
Max Magnitude0
ClinVar
Risk rs397507637(;)
Alt rs397507637(;)
Reference rs397507637(C;C)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911193delC
CLNSRC ClinVar
CLNACC RCV000044042.3,