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rs397507814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507814(-;-)
Make rs397507814(-;A)
Make rs397507814(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340307
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507814
ebirs397507814
HLIrs397507814
Exacrs397507814
Varsomers397507814
Maprs397507814
PheGenIrs397507814
hapmaprs397507814
1000 genomesrs397507814
hgdprs397507814
ensemblrs397507814
gopubmedrs397507814
geneviewrs397507814
scholarrs397507814
googlers397507814
pharmgkbrs397507814
gwascentralrs397507814
openSNPrs397507814
23andMers397507814
23andMe allrs397507814
SNP Nexus

SNPshotrs397507814
SNPdbers397507814
MSV3drs397507814
GWAS Ctlgrs397507814
Max Magnitude0
ClinVar
Risk rs397507814(A;A)
Alt rs397507814(A;A)
Reference rs397507814(;)
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.32914444dupA
CLNSRC ClinVar
CLNACC RCV000044801.2, RCV000162056.1,