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rs397507575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507575(G;T)
Make rs397507575(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332658
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507575
ebirs397507575
HLIrs397507575
Exacrs397507575
Varsomers397507575
Maprs397507575
PheGenIrs397507575
hapmaprs397507575
1000 genomesrs397507575
hgdprs397507575
ensemblrs397507575
gopubmedrs397507575
geneviewrs397507575
scholarrs397507575
googlers397507575
pharmgkbrs397507575
gwascentralrs397507575
openSNPrs397507575
23andMers397507575
23andMe allrs397507575
SNP Nexus

SNPshotrs397507575
SNPdbers397507575
MSV3drs397507575
GWAS Ctlgrs397507575
Max Magnitude0
ClinVar
Risk rs397507575(T;T)
Alt rs397507575(T;T)
Reference rs397507575(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906795G>T
CLNSRC ClinVar
CLNACC RCV000043751.2,