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rs397508891

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508891(-;-)
Make rs397508891(-;G)
Make rs397508891(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093907
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508891
ebirs397508891
HLIrs397508891
Exacrs397508891
Varsomers397508891
Maprs397508891
PheGenIrs397508891
hapmaprs397508891
1000 genomesrs397508891
hgdprs397508891
ensemblrs397508891
gopubmedrs397508891
geneviewrs397508891
scholarrs397508891
googlers397508891
pharmgkbrs397508891
gwascentralrs397508891
openSNPrs397508891
23andMers397508891
23andMe allrs397508891
SNP Nexus

SNPshotrs397508891
SNPdbers397508891
MSV3drs397508891
GWAS Ctlgrs397508891
Max Magnitude0
ClinVar
Risk rs397508891(G;G)
Alt rs397508891(G;G)
Reference rs397508891(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245925dupC
CLNSRC ClinVar
CLNACC RCV000047544.2,