BRD3 c.1215+1154G>T

Variant ID: 9-136909261-C-A

NM_007371.3(BRD3):c.1215+1154G>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:

Mendelian randomization analysis identified genes pleiotropically associated with central corneal thickness.

Bmc Genomics
Yang, Zhikun Z; Yang, Jingyun J; Liu, Di D; Yu, Weihong W
Publication Date: 2021-07-07

Variant appearance in text: rs457420
PubMed Link: 34233613
Variant Present in the following documents:
  • Main text
  • 12864_2021_Article_7860.pdf
View BVdb publication page