NOS1AP c.177+38481G>T

Variant ID: 1-162162747-G-T

NM_014697.2(NOS1AP):c.177+38481G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits.

Nature Genetics
Benaglio, Paola P; D'Antonio-Chronowska, Agnieszka A; Ma, Wubin W; Yang, Feng F; Young Greenwald, William W WW; Donovan, Margaret K R MKR; DeBoever, Christopher C; Li, He H; Drees, Frauke F; Singhal, Sanghamitra S; Matsui, Hiroko H; van Setten, Jessica J; Sotoodehnia, Nona N; Gaulton, Kyle J KJ; Smith, Erin N EN; D'Antonio, Matteo M; Rosenfeld, Michael G MG; Frazer, Kelly A KA
Publication Date: 2019-10

Variant appearance in text: rs4657167
PubMed Link: 31570892
Variant Present in the following documents:
  • Main text
View BVdb publication page