PRKCQ c.1647+1214A>G

Variant ID: 10-6497422-T-C

NM_006257.3(PRKCQ):c.1647+1214A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Ranking causal variants and associated regions in genome-wide association studies by the support vector machine and random forest.

Nucleic Acids Research
Roshan, Usman U; Chikkagoudar, Satish S; Wei, Zhi Z; Wang, Kai K; Hakonarson, Hakon H
Publication Date: 2011-05

Variant appearance in text: rs586457
PubMed Link: 21317188
Variant Present in the following documents:
  • supp_gkr064_supplementarygkr064.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: rs586457
PubMed Link: 17357082
Variant Present in the following documents:
  • Main text
View BVdb publication page