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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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