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rs397508056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508056(-;-)
Make rs397508056(-;T)
Make rs397508056(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394930
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508056
ebirs397508056
HLIrs397508056
Exacrs397508056
Varsomers397508056
Maprs397508056
PheGenIrs397508056
hapmaprs397508056
1000 genomesrs397508056
hgdprs397508056
ensemblrs397508056
gopubmedrs397508056
geneviewrs397508056
scholarrs397508056
googlers397508056
pharmgkbrs397508056
gwascentralrs397508056
openSNPrs397508056
23andMers397508056
23andMe allrs397508056
SNP Nexus

SNPshotrs397508056
SNPdbers397508056
MSV3drs397508056
GWAS Ctlgrs397508056
Max Magnitude0
ClinVar
Risk rs397508056(T;T)
Alt rs397508056(T;T)
Reference rs397508056(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32969067dupT
CLNSRC ClinVar
CLNACC RCV000045834.2,