SLC22A6 c.921+33C>T

Variant ID: 11-62748699-G-A

NM_153276.2(SLC22A6):c.921+33C>T

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Trends in the Contribution of Genetic Susceptibility Loci to Hyperuricemia and Gout and Associated Novel Mechanisms.

Frontiers In Cell And Developmental Biology
Zhao, Jianan J; Guo, Shicheng S; Schrodi, Steven J SJ; He, Dongyi D
Publication Date: 2022

Variant appearance in text: rs2276300
PubMed Link: 35813212
Variant Present in the following documents:
  • Main text
  • fcell-10-937855.pdf
View BVdb publication page



Functional Characterization of Rare Variants in OAT1/SLC22A6 and OAT3/SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort.

Cells
Vávra, Jiří J; Mančíková, Andrea A; Pavelcová, Kateřina K; Hasíková, Lenka L; Bohatá, Jana J; Stibůrková, Blanka B
Publication Date: 2022-03-22

Variant appearance in text: SLC22A6: 921+33C>T; rs2276300
PubMed Link: 35406626
Variant Present in the following documents:
  • Main text
  • cells-11-01063.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: SLC22A6: 921+33C>T; rs2276300
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Population-Specific Resequencing Associates the ATP-Binding Cassette Subfamily C Member 4 Gene With Gout in New Zealand Māori and Pacific Men.

Arthritis & Rheumatology (Hoboken, N.J.)
Tanner, Callum C; Boocock, James J; Stahl, Eli A EA; Dobbyn, Amanda A; Mandal, Asim K AK; Cadzow, Murray M; Phipps-Green, Amanda J AJ; Topless, Ruth K RK; Hindmarsh, Jennie Harré JH; Stamp, Lisa K LK; Dalbeth, Nicola N; Choi, Hyon K HK; Mount, David B DB; Merriman, Tony R TR
Publication Date: 2017-07

Variant appearance in text: rs2276300
PubMed Link: 28371506
Variant Present in the following documents:
  • Main text
View BVdb publication page



Analysis of pharmacogenetic traits in two distinct South African populations.

Human Genomics
Ikediobi, Ogechi O; Aouizerat, Bradley B; Xiao, Yuanyuan Y; Gandhi, Monica M; Gebhardt, Stefan S; Warnich, Louise L
Publication Date: 2011-05

Variant appearance in text: rs2276300
PubMed Link: 21712189
Variant Present in the following documents:
  • Main text
View BVdb publication page



Torsemide renal clearance and genetic variation in luminal and basolateral organic anion transporters.

British Journal Of Clinical Pharmacology
Vormfelde, Stefan V SV; Schirmer, Markus M; Hagos, Yohannes Y; Toliat, Mohammad R MR; Engelhardt, Sabine S; Meineke, Ingolf I; Burckhardt, Gerhard G; Nürnberg, Peter P; Brockmöller, Jürgen J
Publication Date: 2006-09

Variant appearance in text: rs2276300
PubMed Link: 16934049
Variant Present in the following documents:
  • Main text
View BVdb publication page