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rs397507742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507742(-;-)
Make rs397507742(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339135
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507742
ebirs397507742
HLIrs397507742
Exacrs397507742
Varsomers397507742
Maprs397507742
PheGenIrs397507742
hapmaprs397507742
1000 genomesrs397507742
hgdprs397507742
ensemblrs397507742
gopubmedrs397507742
geneviewrs397507742
scholarrs397507742
googlers397507742
pharmgkbrs397507742
gwascentralrs397507742
openSNPrs397507742
23andMers397507742
23andMe allrs397507742
SNP Nexus

SNPshotrs397507742
SNPdbers397507742
MSV3drs397507742
GWAS Ctlgrs397507742
Max Magnitude0
ClinVar
Risk rs397507742(;)
Alt rs397507742(;)
Reference rs397507742(A;A)
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.32913272delA
CLNSRC ClinVar
CLNACC RCV000044492.2, RCV000164279.1,