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rs397507901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507901(-;-)
Make rs397507901(-;T)
Make rs397507901(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355040
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507901
ebirs397507901
HLIrs397507901
Exacrs397507901
Varsomers397507901
Maprs397507901
PheGenIrs397507901
hapmaprs397507901
1000 genomesrs397507901
hgdprs397507901
ensemblrs397507901
gopubmedrs397507901
geneviewrs397507901
scholarrs397507901
googlers397507901
pharmgkbrs397507901
gwascentralrs397507901
openSNPrs397507901
23andMers397507901
23andMe allrs397507901
SNP Nexus

SNPshotrs397507901
SNPdbers397507901
MSV3drs397507901
GWAS Ctlgrs397507901
Max Magnitude0
ClinVar
Risk rs397507901(T;T)
Alt rs397507901(T;T)
Reference rs397507901(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32929177dupT
CLNSRC ClinVar
CLNACC RCV000045159.2,