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rs397507587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507587(G;T)
Make rs397507587(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332901
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507587
ebirs397507587
HLIrs397507587
Exacrs397507587
Varsomers397507587
Maprs397507587
PheGenIrs397507587
hapmaprs397507587
1000 genomesrs397507587
hgdprs397507587
ensemblrs397507587
gopubmedrs397507587
geneviewrs397507587
scholarrs397507587
googlers397507587
pharmgkbrs397507587
gwascentralrs397507587
openSNPrs397507587
23andMers397507587
23andMe allrs397507587
SNP Nexus

SNPshotrs397507587
SNPdbers397507587
MSV3drs397507587
GWAS Ctlgrs397507587
Max Magnitude0
ClinVar
Risk rs397507587(T;T)
Alt rs397507587(T;T)
Reference rs397507587(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.32907038G>T
CLNSRC ClinVar
CLNACC RCV000043804.2,