CDKAL1 c.1056-21427C>T

Variant ID: 6-21043852-C-T

NM_017774.3(CDKAL1):c.1056-21427C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.

Plos One
Kim, Jeong-Hyun JH; Cheong, Hyun Sub HS; Sul, Jae Hoon JH; Seo, Jeong-Meen JM; Kim, Dae-Yeon DY; Oh, Jung-Tak JT; Park, Kwi-Won KW; Kim, Hyun-Young HY; Jung, Soo-Min SM; Jung, Kyuwhan K; Cho, Min Jeng MJ; Bae, Joon Seol JS; Shin, Hyoung Doo HD
Publication Date: 2014

Variant appearance in text: rs9348455
PubMed Link: 25310821
Variant Present in the following documents:
  • Main text
  • pone.0110292.pdf
View BVdb publication page