rs3816873
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2.2 | reduced risk of type-2 diabetes |
(C;T) | None | |
(T;T) | 0 | None |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 99583507 |
Gene | MTTP |
is a | snp |
is | mentioned by |
dbSNP | rs3816873 |
dbSNP (classic) | rs3816873 |
ClinGen | rs3816873 |
ebi | rs3816873 |
HLI | rs3816873 |
Exac | rs3816873 |
Gnomad | rs3816873 |
Varsome | rs3816873 |
LitVar | rs3816873 |
Map | rs3816873 |
PheGenI | rs3816873 |
Biobank | rs3816873 |
1000 genomes | rs3816873 |
hgdp | rs3816873 |
ensembl | rs3816873 |
geneview | rs3816873 |
scholar | rs3816873 |
rs3816873 | |
pharmgkb | rs3816873 |
gwascentral | rs3816873 |
openSNP | rs3816873 |
23andMe | rs3816873 |
SNPshot | rs3816873 |
SNPdbe | rs3816873 |
MSV3d | rs3816873 |
GWAS Ctlg | rs3816873 |
GMAF | 0.2158 |
Max Magnitude | 2.2 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Also known as I128T MTP
[PMID 16721486] rare allele of the MTP I128T polymorphism may be protective against impaired glucose tolerance, type-2 diabetes
ClinVar | |
---|---|
Risk | Rs3816873(C;C) |
Alt | Rs3816873(C;C) |
Reference | Rs3816873(T;T) |
Significance | Other |
Disease | Metabolic syndrome not specified Abetalipoproteinemia |
Variation | info |
Gene | MTTP |
CLNDBN | Metabolic syndrome, protection against not specified Abetalipoproteinemia |
Reversed | 0 |
HGVS | NC_000004.11:g.100504664T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015310.3, RCV000117636.3, RCV000333725.1, |
[PMID 21438662] Association of polymorphisms in glutamate-cysteine ligase catalytic subunit and microsomal triglyceride transfer protein genes with nonalcoholic fatty liver disease.