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rs397507604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507604(A;A)
Make rs397507604(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333226
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507604
ebirs397507604
HLIrs397507604
Exacrs397507604
Varsomers397507604
Maprs397507604
PheGenIrs397507604
hapmaprs397507604
1000 genomesrs397507604
hgdprs397507604
ensemblrs397507604
gopubmedrs397507604
geneviewrs397507604
scholarrs397507604
googlers397507604
pharmgkbrs397507604
gwascentralrs397507604
openSNPrs397507604
23andMers397507604
23andMe allrs397507604
SNP Nexus

SNPshotrs397507604
SNPdbers397507604
MSV3drs397507604
GWAS Ctlgrs397507604
Max Magnitude0
ClinVar
Risk rs397507604(A;A)
Alt rs397507604(A;A)
Reference rs397507604(T;T)
Significance Pathogenic
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907363T>A
CLNSRC ClinVar
CLNACC RCV000043871.2, RCV000165753.1, RCV000225624.1,