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rs1057519669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 5 Familial Hypercholesterolemia
Chromosome19
Position11113347
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1057519669
dbSNP (classic)rs1057519669
ClinGenrs1057519669
ebirs1057519669
HLIrs1057519669
Exacrs1057519669
Gnomadrs1057519669
Varsomers1057519669
LitVarrs1057519669
Maprs1057519669
PheGenIrs1057519669
Biobankrs1057519669
1000 genomesrs1057519669
hgdprs1057519669
ensemblrs1057519669
geneviewrs1057519669
scholarrs1057519669
googlers1057519669
pharmgkbrs1057519669
gwascentralrs1057519669
openSNPrs1057519669
23andMers1057519669
23andMe allrs1057519669
SNPshotrs1057519669
SNPdbers1057519669
MSV3drs1057519669
GWAS Ctlgrs1057519669
Max Magnitude5
ClinVar
Risk rs1057519669(G;G)
Alt rs1057519669(G;G)
Reference Rs1057519669(A;A)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224023A>G
CLNSRC
CLNACC RCV000417351.1,