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rs397507903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507903(-;-)
Make rs397507903(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319080
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507903
ebirs397507903
HLIrs397507903
Exacrs397507903
Varsomers397507903
Maprs397507903
PheGenIrs397507903
hapmaprs397507903
1000 genomesrs397507903
hgdprs397507903
ensemblrs397507903
gopubmedrs397507903
geneviewrs397507903
scholarrs397507903
googlers397507903
pharmgkbrs397507903
gwascentralrs397507903
openSNPrs397507903
23andMers397507903
23andMe allrs397507903
SNP Nexus

SNPshotrs397507903
SNPdbers397507903
MSV3drs397507903
GWAS Ctlgrs397507903
Max Magnitude0
ClinVar
Risk rs397507903(;)
Alt rs397507903(;)
Reference rs397507903(T;T)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32893217delT
CLNSRC ClinVar
CLNACC RCV000045163.2, RCV000166421.1,