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rs1060499924

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 5 Familial Hypercholesterolemia
Chromosome19
Position11113454
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1060499924
dbSNP (old)rs1060499924
ClinGenrs1060499924
ebirs1060499924
HLIrs1060499924
Exacrs1060499924
Gnomadrs1060499924
Varsomers1060499924
Maprs1060499924
PheGenIrs1060499924
Biobankrs1060499924
1000 genomesrs1060499924
hgdprs1060499924
ensemblrs1060499924
gopubmedrs1060499924
geneviewrs1060499924
scholarrs1060499924
googlers1060499924
pharmgkbrs1060499924
gwascentralrs1060499924
openSNPrs1060499924
23andMers1060499924
23andMe allrs1060499924
SNPshotrs1060499924
SNPdbers1060499924
MSV3drs1060499924
GWAS Ctlgrs1060499924
Max Magnitude5
ClinVar
Risk rs1060499924(T;T)
Alt rs1060499924(T;T)
Reference Rs1060499924(G;G)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11224130G>T
CLNSRC
CLNACC RCV000455239.1,