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rs1057519668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 5 Familial Hypercholesterolemia
(T;T) 0 common in clinvar
Chromosome19
Position11113296
GeneLDLR, MIR6886
is asnp
is mentioned by
dbSNPrs1057519668
dbSNP (old)rs1057519668
ClinGenrs1057519668
ebirs1057519668
HLIrs1057519668
Exacrs1057519668
Gnomadrs1057519668
Varsomers1057519668
Maprs1057519668
PheGenIrs1057519668
Biobankrs1057519668
1000 genomesrs1057519668
hgdprs1057519668
ensemblrs1057519668
gopubmedrs1057519668
geneviewrs1057519668
scholarrs1057519668
googlers1057519668
pharmgkbrs1057519668
gwascentralrs1057519668
openSNPrs1057519668
23andMers1057519668
23andMe allrs1057519668
SNPshotrs1057519668
SNPdbers1057519668
MSV3drs1057519668
GWAS Ctlgrs1057519668
Max Magnitude5
ClinVar
Risk rs1057519668(C;C)
Alt rs1057519668(C;C)
Reference Rs1057519668(T;T)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR MIR6886
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11223972T>C
CLNSRC
CLNACC RCV000417345.1,