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rs397509124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509124(-;-)
Make rs397509124(-;T)
Make rs397509124(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091548
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509124
ebirs397509124
HLIrs397509124
Exacrs397509124
Varsomers397509124
Maprs397509124
PheGenIrs397509124
hapmaprs397509124
1000 genomesrs397509124
hgdprs397509124
ensemblrs397509124
gopubmedrs397509124
geneviewrs397509124
scholarrs397509124
googlers397509124
pharmgkbrs397509124
gwascentralrs397509124
openSNPrs397509124
23andMers397509124
23andMe allrs397509124
SNP Nexus

SNPshotrs397509124
SNPdbers397509124
MSV3drs397509124
GWAS Ctlgrs397509124
Max Magnitude0
ClinVar
Risk rs397509124(T;T)
Alt rs397509124(T;T)
Reference rs397509124(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243566dupA
CLNSRC ClinVar
CLNACC RCV000048400.2,