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rs397507698

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507698(-;-)
Make rs397507698(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338270
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507698
ebirs397507698
HLIrs397507698
Exacrs397507698
Varsomers397507698
Maprs397507698
PheGenIrs397507698
hapmaprs397507698
1000 genomesrs397507698
hgdprs397507698
ensemblrs397507698
gopubmedrs397507698
geneviewrs397507698
scholarrs397507698
googlers397507698
pharmgkbrs397507698
gwascentralrs397507698
openSNPrs397507698
23andMers397507698
23andMe allrs397507698
SNP Nexus

SNPshotrs397507698
SNPdbers397507698
MSV3drs397507698
GWAS Ctlgrs397507698
Max Magnitude0
ClinVar
Risk rs397507698(;)
Alt rs397507698(;)
Reference rs397507698(T;T)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912407delT
CLNSRC ClinVar
CLNACC RCV000044308.2, RCV000162054.1,