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rs397507798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507798(A;G)
Make rs397507798(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326554
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507798
ebirs397507798
HLIrs397507798
Exacrs397507798
Varsomers397507798
Maprs397507798
PheGenIrs397507798
hapmaprs397507798
1000 genomesrs397507798
hgdprs397507798
ensemblrs397507798
gopubmedrs397507798
geneviewrs397507798
scholarrs397507798
googlers397507798
pharmgkbrs397507798
gwascentralrs397507798
openSNPrs397507798
23andMers397507798
23andMe allrs397507798
SNP Nexus

SNPshotrs397507798
SNPdbers397507798
MSV3drs397507798
GWAS Ctlgrs397507798
Max Magnitude0
ClinVar
Risk rs397507798(G,T;G,T)
Alt rs397507798(G,T;G,T)
Reference rs397507798(A;A)
Significance Untested
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.32900691A>G; NC_000013.10:g.32900691A>T
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000044734.2, RCV000044735.2, RCV000129294.2,