PC c.1-36360T>C

Variant ID: 11-66675990-A-G

NM_001040716.1(PC):c.1-36360T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Phenotype-Specific Enrichment of Mendelian Disorder Genes near GWAS Regions across 62 Complex Traits.

American Journal Of Human Genetics
Freund, Malika Kumar MK; Burch, Kathryn S KS; Shi, Huwenbo H; Mancuso, Nicholas N; Kichaev, Gleb G; Garske, Kristina M KM; Pan, David Z DZ; Miao, Zong Z; Mohlke, Karen L KL; Laakso, Markku M; Pajukanta, Päivi P; Pasaniuc, Bogdan B; Arboleda, Valerie A VA
Publication Date: 2018-10-04

Variant appearance in text: rs6591226
PubMed Link: 30290150
Variant Present in the following documents:
  • Main text
View BVdb publication page