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rs397509003

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ATCAA;ATCAA) 0 common in clinvar
Make rs397509003(-;-)
Make rs397509003(-;ATCAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092801
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509003
ebirs397509003
HLIrs397509003
Exacrs397509003
Varsomers397509003
Maprs397509003
PheGenIrs397509003
hapmaprs397509003
1000 genomesrs397509003
hgdprs397509003
ensemblrs397509003
gopubmedrs397509003
geneviewrs397509003
scholarrs397509003
googlers397509003
pharmgkbrs397509003
gwascentralrs397509003
openSNPrs397509003
23andMers397509003
23andMe allrs397509003
SNP Nexus

SNPshotrs397509003
SNPdbers397509003
MSV3drs397509003
GWAS Ctlgrs397509003
Max Magnitude0
ClinVar
Risk rs397509003(;)
Alt rs397509003(;)
Reference rs397509003(ATCAA;ATCAA)
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.41244818_41244822delTTGAT
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000047945.2, RCV000111923.1,