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rs7754561

From SNPedia

Orientationplus
Stabilizedplus
Make rs7754561(A;A)
Make rs7754561(A;G)
Make rs7754561(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position131891554
GeneENPP1
is asnp
is mentioned by
dbSNPrs7754561
ebirs7754561
HLIrs7754561
Exacrs7754561
Varsomers7754561
Maprs7754561
PheGenIrs7754561
hapmaprs7754561
1000 genomesrs7754561
hgdprs7754561
ensemblrs7754561
gopubmedrs7754561
geneviewrs7754561
scholarrs7754561
googlers7754561
pharmgkbrs7754561
gwascentralrs7754561
openSNPrs7754561
23andMers7754561
23andMe allrs7754561
SNP Nexus

SNPshotrs7754561
SNPdbers7754561
MSV3drs7754561
GWAS Ctlgrs7754561
GMAF0.4894
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19656007OA-icon.png] 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 18304332OA-icon.png] No evidence for association between BMI and 10 candidate genes at ages 4, 7 and 10 in a large UK sample of twins.


[PMID 18426862OA-icon.png] 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 18678618OA-icon.png] Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes.


[PMID 18719658OA-icon.png] Gender differences in the relationship of ENPP1/PC-1 variants to obesity in a Turkish population.


[PMID 19593725OA-icon.png] 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
Variation info
Gene ENPP1
CLNDBN Obesity
Reversed 0
HGVS NC_000006.11:g.132212694A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022719.3,