Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509027

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509027(-;-)
Make rs397509027(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092576
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509027
ebirs397509027
HLIrs397509027
Exacrs397509027
Varsomers397509027
Maprs397509027
PheGenIrs397509027
hapmaprs397509027
1000 genomesrs397509027
hgdprs397509027
ensemblrs397509027
gopubmedrs397509027
geneviewrs397509027
scholarrs397509027
googlers397509027
pharmgkbrs397509027
gwascentralrs397509027
openSNPrs397509027
23andMers397509027
23andMe allrs397509027
SNP Nexus

SNPshotrs397509027
SNPdbers397509027
MSV3drs397509027
GWAS Ctlgrs397509027
Max Magnitude0
ClinVar
Risk rs397509027(;)
Alt rs397509027(;)
Reference rs397509027(C;C)
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.41244593delG
CLNSRC ClinVar
CLNACC RCV000048023.2, RCV000083192.2,