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rs869320651

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320651(A;A)
Make rs869320651(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11113343
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs869320651
ebirs869320651
HLIrs869320651
Exacrs869320651
Varsomers869320651
Maprs869320651
PheGenIrs869320651
hapmaprs869320651
1000 genomesrs869320651
hgdprs869320651
ensemblrs869320651
gopubmedrs869320651
geneviewrs869320651
scholarrs869320651
googlers869320651
pharmgkbrs869320651
gwascentralrs869320651
openSNPrs869320651
23andMers869320651
23andMe allrs869320651
SNP Nexus

SNPshotrs869320651
SNPdbers869320651
MSV3drs869320651
GWAS Ctlgrs869320651
Max Magnitude0
ClinVar
Risk rs869320651(A;A)
Alt rs869320651(A;A)
Reference rs869320651(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224019G>A; NC_000019.9:g.11224019G>T
CLNSRC LDLR @ LOVD
CLNACC RCV000210833.2, RCV000238348.1,