SLC2A9 c.681+15739C>T

Variant ID: 4-9966477-G-A

NM_020041.2(SLC2A9):c.681+15739C>T

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Weak Association Between Genetic Markers of Hyperuricemia and Cardiorenal Outcomes: Insights From the STANISLAS Study Cohort With a 20-Year Follow-Up.

Journal Of The American Heart Association
Kanbay, Mehmet M; Xhaard, Constance C; Le Floch, Edith E; Dandine-Roulland, Claire C; Girerd, Nicolas N; Ferreira, João Pedro JP; Boivin, Jean-Marc JM; Wagner, Sandra S; Bacq-Daian, Delphine D; Deleuze, Jean-François JF; Zannad, Faiez F; Rossignol, Patrick P
Publication Date: 2022-05-03

Variant appearance in text: rs9998811
PubMed Link: 35470676
Variant Present in the following documents:
  • Main text
  • JAH3-11-e023301.pdf
View BVdb publication page



Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals.

American Journal Of Human Genetics
Hivert, Valentin V; Sidorenko, Julia J; Rohart, Florian F; Goddard, Michael E ME; Yang, Jian J; Wray, Naomi R NR; Yengo, Loic L; Visscher, Peter M PM
Publication Date: 2021-05-06

Variant appearance in text: rs9998811
PubMed Link: 33811805
Variant Present in the following documents:
  • Main text
View BVdb publication page



Systemic Investigation of Promoter-wide Methylome and Genome Variations in Gout.

International Journal Of Molecular Sciences
Tseng, Chia-Chun CC; Wong, Man Chun MC; Liao, Wei-Ting WT; Chen, Chung-Jen CJ; Lee, Su-Chen SC; Yen, Jeng-Hsien JH; Chang, Shun-Jen SJ
Publication Date: 2020-07-01

Variant appearance in text: rs9998811
PubMed Link: 32630231
Variant Present in the following documents:
  • ijms-21-04702-s001.pdf
View BVdb publication page



Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study.

Scientific Reports
Chittoor, Geetha G; Haack, Karin K; Balakrishnan, Poojitha P; Bizon, Christopher C; Laston, Sandra S; Best, Lyle G LG; MacCluer, Jean W JW; North, Kari E KE; Umans, Jason G JG; Franceschini, Nora N; Prasad, Gauri G; Macias-Kauffer, Luis L; Villarreal-Molina, Teresa T; Bharadwaj, Dwaipayan D; Canizales-Quinteros, Samuel S; Navas-Acien, Ana A; Cole, Shelley A SA; Voruganti, V S VS
Publication Date: 2019-11-29

Variant appearance in text: rs9998811
PubMed Link: 31784582
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_52924.pdf
View BVdb publication page



Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.

Frontiers In Genetics
Laston, Sandra L SL; Voruganti, V Saroja VS; Haack, Karin K; Shah, Vallabh O VO; Bobelu, Arlene A; Bobelu, Jeanette J; Ghahate, Donica D; Harford, Antonia M AM; Paine, Susan S SS; Tentori, Francesca F; Cole, Shelley A SA; MacCluer, Jean W JW; Comuzzie, Anthony G AG; Zager, Philip G PG
Publication Date: 2015

Variant appearance in text: rs9998811
PubMed Link: 25688259
Variant Present in the following documents:
  • Main text
  • fgene-06-00006.pdf
View BVdb publication page



SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.

European Journal Of Human Genetics : Ejhg
Meirelles, Osorio D OD; Ding, Jun J; Tanaka, Toshiko T; Sanna, Serena S; Yang, Hsih-Te HT; Dudekula, Dawood B DB; Cucca, Francesco F; Ferrucci, Luigi L; Abecasis, Goncalo G; Schlessinger, David D
Publication Date: 2013-06

Variant appearance in text: rs9998811
PubMed Link: 23092954
Variant Present in the following documents:
  • Main text
View BVdb publication page