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rs397509126

From SNPedia

Merged intors80357568
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
dbSNP (classic)rs397509126
ClinGenrs397509126
ebirs397509126
HLIrs397509126
Exacrs397509126
Gnomadrs397509126
Varsomers397509126
LitVarrs397509126
Maprs397509126
PheGenIrs397509126
Biobankrs397509126
1000 genomesrs397509126
hgdprs397509126
ensemblrs397509126
geneviewrs397509126
scholarrs397509126
googlers397509126
pharmgkbrs397509126
gwascentralrs397509126
openSNPrs397509126
23andMers397509126
SNPshotrs397509126
SNPdbers397509126
MSV3drs397509126
GWAS Ctlgrs397509126
StatusMerged into rs80357568
Max Magnitude0
ClinVar
Risk
Alt
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, RCV000112478.2,