PRKCA c.205+94735C>T

Variant ID: 17-64396980-C-T

NM_002737.2(PRKCA):c.205+94735C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs4561502
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



PRKCA and multiple sclerosis: association in two independent populations.

Plos Genetics
Saarela, Janna J; Kallio, Suvi P SP; Chen, Daniel D; Montpetit, Alexandre A; Jokiaho, Anne A; Choi, Eva E; Asselta, Rosanna R; Bronnikov, Denis D; Lincoln, Matthew R MR; Sadovnick, A Dessa AD; Tienari, Pentti J PJ; Koivisto, Keijo K; Palotie, Aarno A; Ebers, George C GC; Hudson, Thomas J TJ; Peltonen, Leena L
Publication Date: 2006-03

Variant appearance in text: rs4561502
PubMed Link: 16596167
Variant Present in the following documents:
  • Main text
  • pgen.0020042.pdf
View BVdb publication page