DMD c.531-1108A>T

Variant ID: X-32828836-T-A

NM_004006.2(DMD):c.531-1108A>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs1158629
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



Unrecognized sequence homologies may confound genome-wide association studies.

Nucleic Acids Research
Galichon, Pierre P; Mesnard, Laurent L; Hertig, Alexandre A; Stengel, Bénédicte B; Rondeau, Eric E
Publication Date: 2012-06

Variant appearance in text: rs1158629
PubMed Link: 22362730
Variant Present in the following documents:
  • Main text
  • gks169.pdf
View BVdb publication page