CMIP c.300+54643C>G

Variant ID: 16-81533789-C-G

NM_198390.2(CMIP):c.300+54643C>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Pleiotropic genetic architecture and novel loci for C-reactive protein levels.

Nature Communications
Koskeridis, Fotios F; Evangelou, Evangelos E; Said, Saredo S; Boyle, Joseph J JJ; Elliott, Paul P; Dehghan, Abbas A; Tzoulaki, Ioanna I
Publication Date: 2022-11-14

Variant appearance in text: rs56823429
PubMed Link: 36376304
Variant Present in the following documents:
  • Main text
View BVdb publication page



The association of the CMIP rs16955379 polymorphism with dyslipidemia and the clinicopathological features of IgA nephropathy.

International Journal Of Clinical And Experimental Pathology
Mo, Man-Qiu MQ; Pan, Ling L; Lu, Qing-Mei QM; Li, Qiu-Lin QL; Liao, Yun-Hua YH
Publication Date: 2018

Variant appearance in text: rs56823429
PubMed Link: 31949578
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.

Genetic Epidemiology
Keaton, Jacob M JM; Gao, Chuan C; Guan, Meijian M; Hellwege, Jacklyn N JN; Palmer, Nicholette D ND; Pankow, James S JS; Fornage, Myriam M; Wilson, James G JG; Correa, Adolfo A; Rasmussen-Torvik, Laura J LJ; Rotter, Jerome I JI; Chen, Yii-Der I YI; Taylor, Kent D KD; Rich, Stephen S SS; Wagenknecht, Lynne E LE; Freedman, Barry I BI; Ng, Maggie C Y MCY; Bowden, Donald W DW
Publication Date: 2018-09

Variant appearance in text: rs56823429
PubMed Link: 29691896
Variant Present in the following documents:
  • Main text
View BVdb publication page