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rs879254870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 5 Familial Hypercholesterolemia
Make rs879254870(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position11113431
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs879254870
dbSNP (classic)rs879254870
ClinGenrs879254870
ebirs879254870
HLIrs879254870
Exacrs879254870
Gnomadrs879254870
Varsomers879254870
LitVarrs879254870
Maprs879254870
PheGenIrs879254870
Biobankrs879254870
1000 genomesrs879254870
hgdprs879254870
ensemblrs879254870
geneviewrs879254870
scholarrs879254870
googlers879254870
pharmgkbrs879254870
gwascentralrs879254870
openSNPrs879254870
23andMers879254870
SNPshotrs879254870
SNPdbers879254870
MSV3drs879254870
GWAS Ctlgrs879254870
Max Magnitude5
ClinVar
Risk rs879254870(G;G)
Alt rs879254870(G;G)
Reference Rs879254870(C;C)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224107C>G
CLNSRC LDLR @ LOVD
CLNACC RCV000237999.1,