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rs397507318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507318(-;-)
Make rs397507318(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32325148
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507318
ebirs397507318
HLIrs397507318
Exacrs397507318
Varsomers397507318
Maprs397507318
PheGenIrs397507318
hapmaprs397507318
1000 genomesrs397507318
hgdprs397507318
ensemblrs397507318
gopubmedrs397507318
geneviewrs397507318
scholarrs397507318
googlers397507318
pharmgkbrs397507318
gwascentralrs397507318
openSNPrs397507318
23andMers397507318
23andMe allrs397507318
SNP Nexus

SNPshotrs397507318
SNPdbers397507318
MSV3drs397507318
GWAS Ctlgrs397507318
Max Magnitude0
ClinVar
Risk rs397507318(;)
Alt rs397507318(;)
Reference rs397507318(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32899285delT
CLNSRC ClinVar
CLNACC RCV000031445.3,