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rs397509019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;TT) 6 BRCA1 variant considered pathogenic for breast cancer
(TT;TT) 0 common in clinvar


Make rs397509019(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092674
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509019
dbSNP (old)rs397509019
ClinGenrs397509019
ebirs397509019
HLIrs397509019
Exacrs397509019
Gnomadrs397509019
Varsomers397509019
Maprs397509019
PheGenIrs397509019
Biobankrs397509019
1000 genomesrs397509019
hgdprs397509019
ensemblrs397509019
gopubmedrs397509019
geneviewrs397509019
scholarrs397509019
googlers397509019
pharmgkbrs397509019
gwascentralrs397509019
openSNPrs397509019
23andMers397509019
23andMe allrs397509019
SNP Nexus

SNPshotrs397509019
SNPdbers397509019
MSV3drs397509019
GWAS Ctlgrs397509019
Max Magnitude6
ClinVar
Risk rs397509019(-;-)
Alt rs397509019(-;-)
Reference Rs397509019(TT;TT)
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.41244691_41244692delAA
CLNSRC ClinVar
CLNACC RCV000047991.2, RCV000256568.2,