DSCAML1 c.511+4242C>T

Variant ID: 11-117643264-G-A

NM_020693.4(DSCAML1):c.511+4242C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.

Nature Communications
Southam, Lorraine L; Gilly, Arthur A; Süveges, Dániel D; Farmaki, Aliki-Eleni AE; Schwartzentruber, Jeremy J; Tachmazidou, Ioanna I; Matchan, Angela A; Rayner, Nigel W NW; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Xue, Yali Y; Dedoussis, George G; Zeggini, Eleftheria E
Publication Date: 2017-05-26

Variant appearance in text: rs145556679
PubMed Link: 28548082
Variant Present in the following documents:
  • Main text
  • ncomms15606-s1.pdf
  • ncomms15606.pdf
  • ncomms15606-s2.pdf
View BVdb publication page