UGT1A3 c.1021_1022delinsTG ;(p.T341C)

Variant ID: 2-234676516-AC-TG

NM_019093.2(UGT1A3):c.1021_1022delinsTG;(p.T341C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene.

World Journal Of Gastroenterology
Machida, Haruhisa H; Tsukamoto, Kazuhiro K; Wen, Chun-Yang CY; Shikuwa, Saburou S; Isomoto, Hajime H; Mizuta, Yohei Y; Takeshima, Fuminao F; Murase, Kunihiko K; Matsumoto, Naomichi N; Murata, Ikuo I; Kohno, Shigeru S; Wen, Chen-Yang CY
Publication Date: 2005-08-21

Variant appearance in text: UGT1A3: T341C
PubMed Link: 16097053
Variant Present in the following documents:
  • Main text
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