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

rs139507589

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139507589(A;A)
Make rs139507589(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11106628
GeneLDLR
is asnp
is mentioned by
dbSNPrs139507589
ebirs139507589
HLIrs139507589
Exacrs139507589
Varsomers139507589
Maprs139507589
PheGenIrs139507589
hapmaprs139507589
1000 genomesrs139507589
hgdprs139507589
ensemblrs139507589
gopubmedrs139507589
geneviewrs139507589
scholarrs139507589
googlers139507589
pharmgkbrs139507589
gwascentralrs139507589
openSNPrs139507589
23andMers139507589
23andMe allrs139507589
SNP Nexus

SNPshotrs139507589
SNPdbers139507589
MSV3drs139507589
GWAS Ctlgrs139507589
Max Magnitude0
ClinVar
Risk rs139507589(A,C;A,C)
Alt rs139507589(A,C;A,C)
Reference rs139507589(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11217304G>C
CLNSRC LDLR @ LOVD
CLNACC RCV000238279.1,