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rs397509061

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509061(-;-)
Make rs397509061(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092154
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509061
ebirs397509061
HLIrs397509061
Exacrs397509061
Varsomers397509061
Maprs397509061
PheGenIrs397509061
hapmaprs397509061
1000 genomesrs397509061
hgdprs397509061
ensemblrs397509061
gopubmedrs397509061
geneviewrs397509061
scholarrs397509061
googlers397509061
pharmgkbrs397509061
gwascentralrs397509061
openSNPrs397509061
23andMers397509061
23andMe allrs397509061
SNP Nexus

SNPshotrs397509061
SNPdbers397509061
MSV3drs397509061
GWAS Ctlgrs397509061
Max Magnitude0
ClinVar
Risk rs397509061(;)
Alt rs397509061(;)
Reference rs397509061(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.41244171delG
CLNSRC ClinVar
CLNACC RCV000048172.2,