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AKAP13 c.5289+2186C>T
Variant ID: 15-86230290-C-T
NM_007200.4(
AKAP13
):c.5289+2186C>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
The Lancet. Respiratory Medicine
Allen, Richard J RJ; Porte, Joanne J; Braybrooke, Rebecca R; Flores, Carlos C; Fingerlin, Tasha E TE; Oldham, Justin M JM; Guillen-Guio, Beatriz B; Ma, Shwu-Fan SF; Okamoto, Tsukasa T; John, Alison E AE; Obeidat, Ma'en M; Yang, Ivana V IV; Henry, Amanda A; Hubbard, Richard B RB; Navaratnam, Vidya V; Saini, Gauri G; Thompson, Norma N; Booth, Helen L HL; Hart, Simon P SP; Hill, Mike R MR; Hirani, Nik N; Maher, Toby M TM; McAnulty, Robin J RJ; Millar, Ann B AB; Molyneaux, Philip L PL; Parfrey, Helen H; Rassl, Doris M DM; Whyte, Moira K B MKB; Fahy, William A WA; Marshall, Richard P RP; Oballa, Eunice E; Bossé, Yohan Y; Nickle, David C DC; Sin, Don D DD; Timens, Wim W; Shrine, Nick N; Sayers, Ian I; Hall, Ian P IP; Noth, Imre I; Schwartz, David A DA; Tobin, Martin D MD; Wain, Louise V LV; Jenkins, R Gisli RG
Publication Date: 2017-11
Variant appearance in text: rs17636666
PubMed Link:
29066090
Variant Present in the following documents:
Main text
View BVdb publication page