PRICKLE1 c.775+408G>A

Variant ID: 12-42859588-C-T

NM_153026.2(PRICKLE1):c.775+408G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Childhood adiposity and novel subtypes of adult-onset diabetes: a Mendelian randomisation and genome-wide genetic correlation study.

Diabetologia
Wei, Yuxia Y; Richardson, Tom G TG; Zhan, Yiqiang Y; Carlsson, Sofia S
Publication Date: 2023-02-27

Variant appearance in text: rs11832772
PubMed Link: 36843089
Variant Present in the following documents:
  • 125_2023_5883_MOESM1_ESM.pdf
View BVdb publication page



Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

American Journal Of Human Genetics
Melquist, Stacey S; Craig, David W DW; Huentelman, Matthew J MJ; Crook, Richard R; Pearson, John V JV; Baker, Matt M; Zismann, Victoria L VL; Gass, Jennifer J; Adamson, Jennifer J; Szelinger, Szabolcs S; Corneveaux, Jason J; Cannon, Ashley A; Coon, Keith D KD; Lincoln, Sarah S; Adler, Charles C; Tuite, Paul P; Calne, Donald B DB; Bigio, Eileen H EH; Uitti, Ryan J RJ; Wszolek, Zbigniew K ZK; Golbe, Lawrence I LI; Caselli, Richard J RJ; Graff-Radford, Neill N; Litvan, Irene I; Farrer, Matthew J MJ; Dickson, Dennis W DW; Hutton, Mike M; Stephan, Dietrich A DA
Publication Date: 2007-04

Variant appearance in text: rs11832772
PubMed Link: 17357082
Variant Present in the following documents:
  • Main text
View BVdb publication page