PRKCA c.288+59414C>G

Variant ID: 17-64551815-C-G

NM_002737.2(PRKCA):c.288+59414C>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Replication analysis of variants associated with multiple sclerosis risk.

Scientific Reports
Dashti, Mohammad M; Ateyah, Khadijah K; Alroughani, Raed R; Al-Temaimi, Rabeah R
Publication Date: 2020-04-30

Variant appearance in text: rs2078153
PubMed Link: 32355262
Variant Present in the following documents:
  • 41598_2020_64432_MOESM1_ESM.pdf
View BVdb publication page



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: rs2078153
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: rs2078153
PubMed Link: 16596167
Variant Present in the following documents:
  • Main text
  • pgen.0020042.pdf
View BVdb publication page