IGF1R c.1248-536A>C

Variant ID: 15-99451378-A-C

NM_000875.3(IGF1R):c.1248-536A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs8039666
PubMed Link: 21304894
Variant Present in the following documents:
  • Main text
  • pgen.1001293.pdf
View BVdb publication page