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

rs397509240

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509240(-;-)
Make rs397509240(-;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057099
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509240
ebirs397509240
HLIrs397509240
Exacrs397509240
Varsomers397509240
Maprs397509240
PheGenIrs397509240
hapmaprs397509240
1000 genomesrs397509240
hgdprs397509240
ensemblrs397509240
gopubmedrs397509240
geneviewrs397509240
scholarrs397509240
googlers397509240
pharmgkbrs397509240
gwascentralrs397509240
openSNPrs397509240
23andMers397509240
23andMe allrs397509240
SNP Nexus

SNPshotrs397509240
SNPdbers397509240
MSV3drs397509240
GWAS Ctlgrs397509240
Max Magnitude0
ClinVar
Risk rs397509240(;)
Alt rs397509240(;)
Reference rs397509240(A;A)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41209116delT
CLNSRC ClinVar
CLNACC RCV000048872.2, RCV000217310.1,