ALK c.1282+1621C>A

Variant ID: 2-29604977-G-T

NM_004304.4(ALK):c.1282+1621C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.

Plos Genetics
Tiensuu, Heli H; Haapalainen, Antti M AM; Karjalainen, Minna K MK; Pasanen, Anu A; Huusko, Johanna M JM; Marttila, Riitta R; Ojaniemi, Marja M; Muglia, Louis J LJ; Hallman, Mikko M; Rämet, Mika M
Publication Date: 2019-06

Variant appearance in text: rs7608573
PubMed Link: 31194736
Variant Present in the following documents:
  • Main text
  • pgen.1008107.pdf
View BVdb publication page



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: rs7608573
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page