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rs1060499922

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TG) 5 Familial Hypercholesterolemia
(TG;TG) 0 common in clinvar
Chromosome19
Position11111637
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1060499922
dbSNP (old)rs1060499922
ClinGenrs1060499922
ebirs1060499922
HLIrs1060499922
Exacrs1060499922
Gnomadrs1060499922
Varsomers1060499922
Maprs1060499922
PheGenIrs1060499922
Biobankrs1060499922
1000 genomesrs1060499922
hgdprs1060499922
ensemblrs1060499922
gopubmedrs1060499922
geneviewrs1060499922
scholarrs1060499922
googlers1060499922
pharmgkbrs1060499922
gwascentralrs1060499922
openSNPrs1060499922
23andMers1060499922
23andMe allrs1060499922
SNPshotrs1060499922
SNPdbers1060499922
MSV3drs1060499922
GWAS Ctlgrs1060499922
Max Magnitude5
ClinVar
Risk rs1060499922(-;-)
Alt rs1060499922(-;-)
Reference Rs1060499922(TG;TG)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11222313_11222314delTG
CLNSRC
CLNACC RCV000455355.1,