rs7754561
Orientation | plus |
Stabilized | plus |
Make rs7754561(A;A) |
Make rs7754561(A;G) |
Make rs7754561(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 131891554 |
Gene | ENPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs7754561 |
dbSNP (classic) | rs7754561 |
ClinGen | rs7754561 |
ebi | rs7754561 |
HLI | rs7754561 |
Exac | rs7754561 |
Gnomad | rs7754561 |
Varsome | rs7754561 |
LitVar | rs7754561 |
Map | rs7754561 |
PheGenI | rs7754561 |
Biobank | rs7754561 |
1000 genomes | rs7754561 |
hgdp | rs7754561 |
ensembl | rs7754561 |
geneview | rs7754561 |
scholar | rs7754561 |
rs7754561 | |
pharmgkb | rs7754561 |
gwascentral | rs7754561 |
openSNP | rs7754561 |
23andMe | rs7754561 |
SNPshot | rs7754561 |
SNPdbe | rs7754561 |
MSV3d | rs7754561 |
GWAS Ctlg | rs7754561 |
GMAF | 0.4894 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19656007] Genetic Variants of the ENPP1/PC-1 Gene Are Associated with Hypertriglyceridemia in Male Subjects
[PMID 17065359] Common variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity.
[PMID 17704904] ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study.
[PMID 18304332] No evidence for association between BMI and 10 candidate genes at ages 4, 7 and 10 in a large UK sample of twins.
[PMID 18426862] Haplotype structure of the ENPP1 Gene and Nominal Association of the K121Q missense single nucleotide polymorphism with glycemic traits in the Framingham Heart Study.
[PMID 18678618] Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes.
[PMID 18719658] Gender differences in the relationship of ENPP1/PC-1 variants to obesity in a Turkish population.
[PMID 19593725] Association of maternally inherited GNAS alleles with African-American male birth weight.
[PMID 20981035] The ENPP1 K121Q polymorphism is not associated with type 2 diabetes or obesity in the Chinese Han population.
ClinVar | |
---|---|
Risk | rs7754561(G;G) |
Alt | rs7754561(G;G) |
Reference | rs7754561(A;A) |
Significance | Other |
Disease | Obesity Arterial calcification of infancy Hypophosphatemic Rickets |
Variation | info |
Gene | ENPP1 |
CLNDBN | Obesity Arterial calcification of infancy Hypophosphatemic Rickets, Recessive |
Reversed | 0 |
HGVS | NC_000006.11:g.132212694A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000022719.3, RCV000280683.1, RCV000372927.1, |