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rs397507437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507437(-;-)
Make rs397507437(-;T)
Make rs397507437(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332476
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507437
ebirs397507437
HLIrs397507437
Exacrs397507437
Varsomers397507437
Maprs397507437
PheGenIrs397507437
hapmaprs397507437
1000 genomesrs397507437
hgdprs397507437
ensemblrs397507437
gopubmedrs397507437
geneviewrs397507437
scholarrs397507437
googlers397507437
pharmgkbrs397507437
gwascentralrs397507437
openSNPrs397507437
23andMers397507437
23andMe allrs397507437
SNP Nexus

SNPshotrs397507437
SNPdbers397507437
MSV3drs397507437
GWAS Ctlgrs397507437
Max Magnitude0
ClinVar
Risk rs397507437(T;T)
Alt rs397507437(T;T)
Reference rs397507437(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32906613dupT
CLNSRC ClinVar
CLNACC RCV000031850.3,