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rs397507317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507317(-;-)
Make rs397507317(-;T)
Make rs397507317(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338203
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507317
ebirs397507317
HLIrs397507317
Exacrs397507317
Varsomers397507317
Maprs397507317
PheGenIrs397507317
hapmaprs397507317
1000 genomesrs397507317
hgdprs397507317
ensemblrs397507317
gopubmedrs397507317
geneviewrs397507317
scholarrs397507317
googlers397507317
pharmgkbrs397507317
gwascentralrs397507317
openSNPrs397507317
23andMers397507317
23andMe allrs397507317
SNP Nexus

SNPshotrs397507317
SNPdbers397507317
MSV3drs397507317
GWAS Ctlgrs397507317
Max Magnitude0
ClinVar
Risk rs397507317(T;T)
Alt rs397507317(T;T)
Reference rs397507317(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912340dupT
CLNSRC ClinVar
CLNACC RCV000031441.3,