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

rs875989921

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989921(A;A)
Make rs875989921(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113624
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs875989921
ebirs875989921
HLIrs875989921
Exacrs875989921
Varsomers875989921
Maprs875989921
PheGenIrs875989921
hapmaprs875989921
1000 genomesrs875989921
hgdprs875989921
ensemblrs875989921
gopubmedrs875989921
geneviewrs875989921
scholarrs875989921
googlers875989921
pharmgkbrs875989921
gwascentralrs875989921
openSNPrs875989921
23andMers875989921
23andMe allrs875989921
SNP Nexus

SNPshotrs875989921
SNPdbers875989921
MSV3drs875989921
GWAS Ctlgrs875989921
Max Magnitude0
ClinVar
Risk rs875989921(A;A)
Alt rs875989921(A;A)
Reference rs875989921(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224300G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000211662.2,