SCN5A c.935-199T>G

Variant ID: 3-38649904-A-C

NM_000335.4(SCN5A):c.935-199T>G

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: rs13315133
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.

Blood
Galarneau, Geneviève G; Coady, Sean S; Garrett, Melanie E ME; Jeffries, Neal N; Puggal, Mona M; Paltoo, Dina D; Soldano, Karen K; Guasch, Antonio A; Ashley-Koch, Allison E AE; Telen, Marilyn J MJ; Kutlar, Abdullah A; Lettre, Guillaume G; Papanicolaou, George J GJ
Publication Date: 2013-07-18

Variant appearance in text: rs13315133
PubMed Link: 23719301
Variant Present in the following documents:
  • Main text
View BVdb publication page