IGF1R c.641-20151G>C

Variant ID: 15-99414403-G-C

NM_000875.3(IGF1R):c.641-20151G>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Spontaneous preterm birth: the underpinnings in the maternal and fetal genomes.

Npj Genomic Medicine
Bhattacharjee, Esha E; Maitra, Arindam A
Publication Date: 2021-06-08

Variant appearance in text: rs1521480
PubMed Link: 34103530
Variant Present in the following documents:
  • Main text
  • 41525_2021_Article_209.pdf
View BVdb publication page



Candidate gene linkage approach to identify DNA variants that predispose to preterm birth.

Pediatric Research
Bream, Elise N A EN; Leppellere, Cara R CR; Cooper, Margaret E ME; Dagle, John M JM; Merrill, David C DC; Christensen, Kaare K; Simhan, Hyagriv N HN; Fong, Chin-To CT; Hallman, Mikko M; Muglia, Louis J LJ; Marazita, Mary L ML; Murray, Jeffrey C JC
Publication Date: 2013-02

Variant appearance in text: rs1521480
PubMed Link: 23168575
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.

Plos Genetics
Haataja, Ritva R; Karjalainen, Minna K MK; Luukkonen, Aino A; Teramo, Kari K; Puttonen, Hilkka H; Ojaniemi, Marja M; Varilo, Teppo T; Chaudhari, Bimal P BP; Plunkett, Jevon J; Murray, Jeffrey C JC; McCarroll, Steven A SA; Peltonen, Leena L; Muglia, Louis J LJ; Palotie, Aarno A; Hallman, Mikko M
Publication Date: 2011-02-03

Variant appearance in text: rs1521480
PubMed Link: 21304894
Variant Present in the following documents:
  • Main text
  • pgen.1001293.pdf
View BVdb publication page