rs1800591
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1800591(G;G) |
Make rs1800591(G;T) |
Make rs1800591(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 99574331 |
Gene | MTTP |
is a | snp |
is | mentioned by |
dbSNP | rs1800591 |
dbSNP (classic) | rs1800591 |
ClinGen | rs1800591 |
ebi | rs1800591 |
HLI | rs1800591 |
Exac | rs1800591 |
Gnomad | rs1800591 |
Varsome | rs1800591 |
LitVar | rs1800591 |
Map | rs1800591 |
PheGenI | rs1800591 |
Biobank | rs1800591 |
1000 genomes | rs1800591 |
hgdp | rs1800591 |
ensembl | rs1800591 |
geneview | rs1800591 |
scholar | rs1800591 |
rs1800591 | |
pharmgkb | rs1800591 |
gwascentral | rs1800591 |
openSNP | rs1800591 |
23andMe | rs1800591 |
SNPshot | rs1800591 |
SNPdbe | rs1800591 |
MSV3d | rs1800591 |
GWAS Ctlg | rs1800591 |
GMAF | 0.2158 |
Max Magnitude | 0 |
[PMID 23609384] Genetic variants of microsomal triglyceride transfer protein (MTTP) are associated with metabolic syndrome in schizophrenic patients treated with atypical antipsychotics
[PMID 24588800] MTP -493G/T Polymorphism and Susceptibility to Nonalcoholic Fatty Liver Disease: A Meta-Analysis [PMID 14615589] Haplotype-based identification of a microsomal transfer protein marker associated with the human lifespan.
[PMID 17854051] Functional analysis of promoter variants in the microsomal triglyceride transfer protein (MTTP) gene.
[PMID 23533563] Novel risk factors for premature peripheral arterial occlusive disease in non-diabetic patients: a case-control study.