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rs875989922

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989922(A;A)
Make rs875989922(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113645
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs875989922
ebirs875989922
HLIrs875989922
Exacrs875989922
Varsomers875989922
Maprs875989922
PheGenIrs875989922
hapmaprs875989922
1000 genomesrs875989922
hgdprs875989922
ensemblrs875989922
gopubmedrs875989922
geneviewrs875989922
scholarrs875989922
googlers875989922
pharmgkbrs875989922
gwascentralrs875989922
openSNPrs875989922
23andMers875989922
23andMe allrs875989922
SNP Nexus

SNPshotrs875989922
SNPdbers875989922
MSV3drs875989922
GWAS Ctlgrs875989922
Max Magnitude0
ClinVar
Risk rs875989922(A,T;A,T)
Alt rs875989922(A,T;A,T)
Reference rs875989922(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224321G>A; NC_000019.9:g.11224321G>T
CLNSRC LDLR @ LOVD
CLNACC RCV000211689.2, RCV000211612.1,