ALK c.1154+69185G>T

Variant ID: 2-29685596-C-A

NM_004304.4(ALK):c.1154+69185G>T

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: rs3923028
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo.

Molecular Psychiatry
Sullivan, P F PF; de Geus, E J C EJ; Willemsen, G G; James, M R MR; Smit, J H JH; Zandbelt, T T; Arolt, V V; Baune, B T BT; Blackwood, D D; Cichon, S S; Coventry, W L WL; Domschke, K K; Farmer, A A; Fava, M M; Gordon, S D SD; He, Q Q; Heath, A C AC; Heutink, P P; Holsboer, F F; Hoogendijk, W J WJ; Hottenga, J J JJ; Hu, Y Y; Kohli, M M; Lin, D D; Lucae, S S; Macintyre, D J DJ; Maier, W W; McGhee, K A KA; McGuffin, P P; Montgomery, G W GW; Muir, W J WJ; Nolen, W A WA; Nöthen, M M MM; Perlis, R H RH; Pirlo, K K; Posthuma, D D; Rietschel, M M; Rizzu, P P; Schosser, A A; Smit, A B AB; Smoller, J W JW; Tzeng, J-Y JY; van Dyck, R R; Verhage, M M; Zitman, F G FG; Martin, N G NG; Wray, N R NR; Boomsma, D I DI; Penninx, B W J H BW
Publication Date: 2009-04

Variant appearance in text: rs3923028
PubMed Link: 19065144
Variant Present in the following documents:
  • Main text
View BVdb publication page