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rs397509097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509097(-;-)
Make rs397509097(-;C)
Make rs397509097(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091814
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509097
ebirs397509097
HLIrs397509097
Exacrs397509097
Varsomers397509097
Maprs397509097
PheGenIrs397509097
hapmaprs397509097
1000 genomesrs397509097
hgdprs397509097
ensemblrs397509097
gopubmedrs397509097
geneviewrs397509097
scholarrs397509097
googlers397509097
pharmgkbrs397509097
gwascentralrs397509097
openSNPrs397509097
23andMers397509097
23andMe allrs397509097
SNP Nexus

SNPshotrs397509097
SNPdbers397509097
MSV3drs397509097
GWAS Ctlgrs397509097
Max Magnitude0
ClinVar
Risk rs397509097(C;C)
Alt rs397509097(C;C)
Reference rs397509097(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243832dupG
CLNSRC ClinVar
CLNACC RCV000048300.2,