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rs397509126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs397509126(-;-)
Make rs397509126(-;TG)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104163
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509126
ebirs397509126
HLIrs397509126
Exacrs397509126
Varsomers397509126
Maprs397509126
PheGenIrs397509126
hapmaprs397509126
1000 genomesrs397509126
hgdprs397509126
ensemblrs397509126
gopubmedrs397509126
geneviewrs397509126
scholarrs397509126
googlers397509126
pharmgkbrs397509126
gwascentralrs397509126
openSNPrs397509126
23andMers397509126
23andMe allrs397509126
SNP Nexus

SNPshotrs397509126
SNPdbers397509126
MSV3drs397509126
GWAS Ctlgrs397509126
Max Magnitude0
ClinVar
Risk rs397509126(;)
Alt rs397509126(;)
Reference rs397509126(TG;TG)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41256180_41256181delCA
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048404.2, RCV000112478.1,