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rs397508890

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508890(-;-)
Make rs397508890(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106508
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508890
ebirs397508890
HLIrs397508890
Exacrs397508890
Varsomers397508890
Maprs397508890
PheGenIrs397508890
hapmaprs397508890
1000 genomesrs397508890
hgdprs397508890
ensemblrs397508890
gopubmedrs397508890
geneviewrs397508890
scholarrs397508890
googlers397508890
pharmgkbrs397508890
gwascentralrs397508890
openSNPrs397508890
23andMers397508890
23andMe allrs397508890
SNP Nexus

SNPshotrs397508890
SNPdbers397508890
MSV3drs397508890
GWAS Ctlgrs397508890
Max Magnitude0
ClinVar
Risk rs397508890(;)
Alt rs397508890(;)
Reference rs397508890(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41258525delG
CLNSRC ClinVar
CLNACC RCV000047540.2,