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rs1060499923

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TT) 5 Familial Hypercholesterolemia
(TT;TT) 0 common in clinvar
Chromosome19
Position11113295
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1060499923
dbSNP (old)rs1060499923
ClinGenrs1060499923
ebirs1060499923
HLIrs1060499923
Exacrs1060499923
Gnomadrs1060499923
Varsomers1060499923
Maprs1060499923
PheGenIrs1060499923
Biobankrs1060499923
1000 genomesrs1060499923
hgdprs1060499923
ensemblrs1060499923
gopubmedrs1060499923
geneviewrs1060499923
scholarrs1060499923
googlers1060499923
pharmgkbrs1060499923
gwascentralrs1060499923
openSNPrs1060499923
23andMers1060499923
23andMe allrs1060499923
SNPshotrs1060499923
SNPdbers1060499923
MSV3drs1060499923
GWAS Ctlgrs1060499923
Max Magnitude5
ClinVar
Risk rs1060499923(-;-)
Alt rs1060499923(-;-)
Reference Rs1060499923(TT;TT)
Significance Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11223971_11223972delTT
CLNSRC
CLNACC RCV000455989.1,