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rs397509169

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509169(-;-)
Make rs397509169(-;C)
Make rs397509169(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076580
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509169
ebirs397509169
HLIrs397509169
Exacrs397509169
Varsomers397509169
Maprs397509169
PheGenIrs397509169
hapmaprs397509169
1000 genomesrs397509169
hgdprs397509169
ensemblrs397509169
gopubmedrs397509169
geneviewrs397509169
scholarrs397509169
googlers397509169
pharmgkbrs397509169
gwascentralrs397509169
openSNPrs397509169
23andMers397509169
23andMe allrs397509169
SNP Nexus

SNPshotrs397509169
SNPdbers397509169
MSV3drs397509169
GWAS Ctlgrs397509169
Max Magnitude0
ClinVar
Risk rs397509169(C;C)
Alt rs397509169(C;C)
Reference rs397509169(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41228598dupG
CLNSRC ClinVar
CLNACC RCV000048548.2,