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rs397507790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507790(-;-)
Make rs397507790(-;A)
Make rs397507790(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339938
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507790
ebirs397507790
HLIrs397507790
Exacrs397507790
Varsomers397507790
Maprs397507790
PheGenIrs397507790
hapmaprs397507790
1000 genomesrs397507790
hgdprs397507790
ensemblrs397507790
gopubmedrs397507790
geneviewrs397507790
scholarrs397507790
googlers397507790
pharmgkbrs397507790
gwascentralrs397507790
openSNPrs397507790
23andMers397507790
23andMe allrs397507790
SNP Nexus

SNPshotrs397507790
SNPdbers397507790
MSV3drs397507790
GWAS Ctlgrs397507790
Max Magnitude0
ClinVar
Risk rs397507790(A;A)
Alt rs397507790(A;A)
Reference rs397507790(;)
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.32914075dupA
CLNSRC ClinVar
CLNACC RCV000044687.2, RCV000166213.1,