RYR2 c.49-20505G>T

Variant ID: 1-237413292-G-T

NM_001035.2(RYR2):c.49-20505G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.

Circulation. Cardiovascular Genetics
Westaway, Shawn K SK; Reinier, Kyndaron K; Huertas-Vazquez, Adriana A; Evanado, Audrey A; Teodorescu, Carmen C; Navarro, Jo J; Sinner, Moritz F MF; Gunson, Karen K; Jui, Jonathan J; Spooner, Peter P; Kaab, Stefan S; Chugh, Sumeet S SS
Publication Date: 2011-08-01

Variant appearance in text: rs888438
PubMed Link: 21685173
Variant Present in the following documents:
  • Main text
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