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rs397507641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs397507641(-;-)
Make rs397507641(-;CT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337129
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507641
ebirs397507641
HLIrs397507641
Exacrs397507641
Varsomers397507641
Maprs397507641
PheGenIrs397507641
hapmaprs397507641
1000 genomesrs397507641
hgdprs397507641
ensemblrs397507641
gopubmedrs397507641
geneviewrs397507641
scholarrs397507641
googlers397507641
pharmgkbrs397507641
gwascentralrs397507641
openSNPrs397507641
23andMers397507641
23andMe allrs397507641
SNP Nexus

SNPshotrs397507641
SNPdbers397507641
MSV3drs397507641
GWAS Ctlgrs397507641
Max Magnitude0
ClinVar
Risk rs397507641(;)
Alt rs397507641(;)
Reference rs397507641(CT;CT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911266_32911267delCT
CLNSRC ClinVar
CLNACC RCV000044054.2,