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rs1064794259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 5 Familial Hypercholesterolemia
Chromosome19
Position11113615
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1064794259
dbSNP (classic)rs1064794259
ClinGenrs1064794259
ebirs1064794259
HLIrs1064794259
Exacrs1064794259
Gnomadrs1064794259
Varsomers1064794259
LitVarrs1064794259
Maprs1064794259
PheGenIrs1064794259
Biobankrs1064794259
1000 genomesrs1064794259
hgdprs1064794259
ensemblrs1064794259
geneviewrs1064794259
scholarrs1064794259
googlers1064794259
pharmgkbrs1064794259
gwascentralrs1064794259
openSNPrs1064794259
23andMers1064794259
23andMe allrs1064794259
SNPshotrs1064794259
SNPdbers1064794259
MSV3drs1064794259
GWAS Ctlgrs1064794259
Max Magnitude5
ClinVar
Risk rs1064794259(T;T)
Alt rs1064794259(T;T)
Reference Rs1064794259(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LDLR MIR6886
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.11224291C>T
CLNSRC
CLNACC RCV000485078.1,