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rs397509009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509009(-;-)
Make rs397509009(-;A)
Make rs397509009(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092781
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509009
ebirs397509009
HLIrs397509009
Exacrs397509009
Varsomers397509009
Maprs397509009
PheGenIrs397509009
hapmaprs397509009
1000 genomesrs397509009
hgdprs397509009
ensemblrs397509009
gopubmedrs397509009
geneviewrs397509009
scholarrs397509009
googlers397509009
pharmgkbrs397509009
gwascentralrs397509009
openSNPrs397509009
23andMers397509009
23andMe allrs397509009
SNP Nexus

SNPshotrs397509009
SNPdbers397509009
MSV3drs397509009
GWAS Ctlgrs397509009
Max Magnitude0
ClinVar
Risk rs397509009(A;A)
Alt rs397509009(A;A)
Reference rs397509009(;)
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.41244799dupT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047957.2, RCV000111931.1,