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

rs878854025

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854025(A;A)
Make rs878854025(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113762
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs878854025
ebirs878854025
HLIrs878854025
Exacrs878854025
Varsomers878854025
Maprs878854025
PheGenIrs878854025
hapmaprs878854025
1000 genomesrs878854025
hgdprs878854025
ensemblrs878854025
gopubmedrs878854025
geneviewrs878854025
scholarrs878854025
googlers878854025
pharmgkbrs878854025
gwascentralrs878854025
openSNPrs878854025
23andMers878854025
23andMe allrs878854025
SNP Nexus

SNPshotrs878854025
SNPdbers878854025
MSV3drs878854025
GWAS Ctlgrs878854025
Max Magnitude0
ClinVar
Risk rs878854025(A;A)
Alt rs878854025(A;A)
Reference rs878854025(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224438G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000231049.2,