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rs879254903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 5 Familial Hypercholesterolemia
(G;G) 0 common in clinvar


Make rs879254903(A;A)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position11113617
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs879254903
dbSNP (classic)rs879254903
ClinGenrs879254903
ebirs879254903
HLIrs879254903
Exacrs879254903
Gnomadrs879254903
Varsomers879254903
LitVarrs879254903
Maprs879254903
PheGenIrs879254903
Biobankrs879254903
1000 genomesrs879254903
hgdprs879254903
ensemblrs879254903
geneviewrs879254903
scholarrs879254903
googlers879254903
pharmgkbrs879254903
gwascentralrs879254903
openSNPrs879254903
23andMers879254903
SNPshotrs879254903
SNPdbers879254903
MSV3drs879254903
GWAS Ctlgrs879254903
Max Magnitude5
ClinVar
Risk rs879254903(A;A)
Alt rs879254903(A;A)
Reference Rs879254903(G;G)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224293G>A
CLNSRC LDLR @ LOVD
CLNACC RCV000237348.1,