PDE5A c.2001-959G>A

Variant ID: 4-120433248-C-T

NM_001083.3(PDE5A):c.2001-959G>A

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:

Identification of novel SNPs associated with coronary artery disease and birth weight using a pleiotropic cFDR method.

Aging
Wu, Xinrui X; Lin, Xu X; Li, Qi Q; Wang, Zun Z; Zhang, Na N; Tian, Mengyuan M; Wang, Xiaolei X; Deng, Hongwen H; Tan, Hongzhuan H
Publication Date: 2020-12-19

Variant appearance in text: rs1480933
PubMed Link: 33411684
Variant Present in the following documents:
  • Main text
  • aging-13-202322.pdf
View BVdb publication page