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rs397509119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509119(-;-)
Make rs397509119(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091605
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509119
ebirs397509119
HLIrs397509119
Exacrs397509119
Varsomers397509119
Maprs397509119
PheGenIrs397509119
hapmaprs397509119
1000 genomesrs397509119
hgdprs397509119
ensemblrs397509119
gopubmedrs397509119
geneviewrs397509119
scholarrs397509119
googlers397509119
pharmgkbrs397509119
gwascentralrs397509119
openSNPrs397509119
23andMers397509119
23andMe allrs397509119
SNP Nexus

SNPshotrs397509119
SNPdbers397509119
MSV3drs397509119
GWAS Ctlgrs397509119
Max Magnitude0
ClinVar
Risk rs397509119(;)
Alt rs397509119(;)
Reference rs397509119(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41243622delT
CLNSRC ClinVar
CLNACC RCV000048381.2,