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rs397509001

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397509001(-;-)
Make rs397509001(-;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092828
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509001
ebirs397509001
HLIrs397509001
Exacrs397509001
Varsomers397509001
Maprs397509001
PheGenIrs397509001
hapmaprs397509001
1000 genomesrs397509001
hgdprs397509001
ensemblrs397509001
gopubmedrs397509001
geneviewrs397509001
scholarrs397509001
googlers397509001
pharmgkbrs397509001
gwascentralrs397509001
openSNPrs397509001
23andMers397509001
23andMe allrs397509001
SNP Nexus

SNPshotrs397509001
SNPdbers397509001
MSV3drs397509001
GWAS Ctlgrs397509001
Max Magnitude0
ClinVar
Risk rs397509001(;)
Alt rs397509001(;)
Reference rs397509001(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.41244845_41244846delAA
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047938.2, RCV000111921.1,