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RORA c.167-71982C>A
Variant ID: 15-61042867-G-T
NM_134261.2(
RORA
):c.167-71982C>A
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
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dbSNP
Publications:
The advances of genetics research on Hirschsprung's disease.
Pediatric Investigation
Ke, Juntao J; Zhu, Ying Y; Miao, Xiaoping X
Publication Date: 2018-09
Variant appearance in text: rs1351544
PubMed Link:
32851260
Variant Present in the following documents:
Main text
PED4-2-189.pdf
View BVdb publication page
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: rs1351544
PubMed Link:
25310821
Variant Present in the following documents:
Main text
pone.0110292.pdf
View BVdb publication page