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rs113669610

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113669610(C;T)
Make rs113669610(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11111557
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs113669610
ebirs113669610
HLIrs113669610
Exacrs113669610
Varsomers113669610
Maprs113669610
PheGenIrs113669610
hapmaprs113669610
1000 genomesrs113669610
hgdprs113669610
ensemblrs113669610
gopubmedrs113669610
geneviewrs113669610
scholarrs113669610
googlers113669610
pharmgkbrs113669610
gwascentralrs113669610
openSNPrs113669610
23andMers113669610
23andMe allrs113669610
SNP Nexus

SNPshotrs113669610
SNPdbers113669610
MSV3drs113669610
GWAS Ctlgrs113669610
Max Magnitude0
ClinVar
Risk rs113669610(T;T)
Alt rs113669610(T;T)
Reference rs113669610(C;C)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222233C>A
CLNSRC LDLR @ LOVD
CLNACC RCV000237222.1,