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rs397509094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACAA;ACAA) 0 common in clinvar
Make rs397509094(-;-)
Make rs397509094(-;ACAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091824
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509094
ebirs397509094
HLIrs397509094
Exacrs397509094
Varsomers397509094
Maprs397509094
PheGenIrs397509094
hapmaprs397509094
1000 genomesrs397509094
hgdprs397509094
ensemblrs397509094
gopubmedrs397509094
geneviewrs397509094
scholarrs397509094
googlers397509094
pharmgkbrs397509094
gwascentralrs397509094
openSNPrs397509094
23andMers397509094
23andMe allrs397509094
SNP Nexus

SNPshotrs397509094
SNPdbers397509094
MSV3drs397509094
GWAS Ctlgrs397509094
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397509094(ACAA;ACAA)
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.41243841_41243844delTTGT
CLNSRC ClinVar
CLNACC RCV000048288.2, RCV000256531.2,