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rs397507572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507572(C;T)
Make rs397507572(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332595
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507572
ebirs397507572
HLIrs397507572
Exacrs397507572
Varsomers397507572
Maprs397507572
PheGenIrs397507572
hapmaprs397507572
1000 genomesrs397507572
hgdprs397507572
ensemblrs397507572
gopubmedrs397507572
geneviewrs397507572
scholarrs397507572
googlers397507572
pharmgkbrs397507572
gwascentralrs397507572
openSNPrs397507572
23andMers397507572
23andMe allrs397507572
SNP Nexus

SNPshotrs397507572
SNPdbers397507572
MSV3drs397507572
GWAS Ctlgrs397507572
Max Magnitude0
ClinVar
Risk rs397507572(T;T)
Alt rs397507572(T;T)
Reference rs397507572(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32906732C>T
CLNSRC ClinVar
CLNACC RCV000043739.2,