PLCL2 c.3205-4529G>A

Variant ID: 3-17126696-G-A

NM_001144382.2(PLCL2):c.3205-4529G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.

European Journal Of Human Genetics : Ejhg
Hirokawa, Megumi M; Morita, Hiroyuki H; Tajima, Tomoyuki T; Takahashi, Atsushi A; Ashikawa, Kyota K; Miya, Fuyuki F; Shigemizu, Daichi D; Ozaki, Kouichi K; Sakata, Yasuhiko Y; Nakatani, Daisaku D; Suna, Shinichiro S; Imai, Yasushi Y; Tanaka, Toshihiro T; Tsunoda, Tatsuhiko T; Matsuda, Koichi K; Kadowaki, Takashi T; Nakamura, Yusuke Y; Nagai, Ryozo R; Komuro, Issei I; Kubo, Michiaki M
Publication Date: 2015-03

Variant appearance in text: rs62248161
PubMed Link: 24916648
Variant Present in the following documents:
  • Main text
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