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rs397507992

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507992(-;-)
Make rs397507992(-;A)
Make rs397507992(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371029
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507992
ebirs397507992
HLIrs397507992
Exacrs397507992
Varsomers397507992
Maprs397507992
PheGenIrs397507992
hapmaprs397507992
1000 genomesrs397507992
hgdprs397507992
ensemblrs397507992
gopubmedrs397507992
geneviewrs397507992
scholarrs397507992
googlers397507992
pharmgkbrs397507992
gwascentralrs397507992
openSNPrs397507992
23andMers397507992
23andMe allrs397507992
SNP Nexus

SNPshotrs397507992
SNPdbers397507992
MSV3drs397507992
GWAS Ctlgrs397507992
Max Magnitude0
ClinVar
Risk rs397507992(A;A)
Alt rs397507992(A;A)
Reference rs397507992(;)
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.32945166dupA
CLNSRC ClinVar
CLNACC RCV000045557.2, RCV000225529.1,