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

rs397509055

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TAAA;TAAA) 0 common in clinvar
Make rs397509055(-;-)
Make rs397509055(-;TAAA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092205
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509055
ebirs397509055
HLIrs397509055
Exacrs397509055
Varsomers397509055
Maprs397509055
PheGenIrs397509055
hapmaprs397509055
1000 genomesrs397509055
hgdprs397509055
ensemblrs397509055
gopubmedrs397509055
geneviewrs397509055
scholarrs397509055
googlers397509055
pharmgkbrs397509055
gwascentralrs397509055
openSNPrs397509055
23andMers397509055
23andMe allrs397509055
SNP Nexus

SNPshotrs397509055
SNPdbers397509055
MSV3drs397509055
GWAS Ctlgrs397509055
Max Magnitude0
ClinVar
Risk rs397509055(;)
Alt rs397509055(;)
Reference rs397509055(TAAA;TAAA)
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.41244222_41244225delTTTA
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048142.2, RCV000112059.1,