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rs397507262

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507262(-;-)
Make rs397507262(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332634
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507262
ebirs397507262
HLIrs397507262
Exacrs397507262
Varsomers397507262
Maprs397507262
PheGenIrs397507262
hapmaprs397507262
1000 genomesrs397507262
hgdprs397507262
ensemblrs397507262
gopubmedrs397507262
geneviewrs397507262
scholarrs397507262
googlers397507262
pharmgkbrs397507262
gwascentralrs397507262
openSNPrs397507262
23andMers397507262
23andMe allrs397507262
SNP Nexus

SNPshotrs397507262
SNPdbers397507262
MSV3drs397507262
GWAS Ctlgrs397507262
Max Magnitude0
ClinVar
Risk rs397507262(;)
Alt rs397507262(;)
Reference rs397507262(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906771delG
CLNSRC ClinVar
CLNACC RCV000031307.3,