SCAF4 c.2043+789A>G

Variant ID: 21-33059831-T-C

NM_020706.2(SCAF4):c.2043+789A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A large electronic-health-record-based genome-wide study of serum lipids.

Nature Genetics
Hoffmann, Thomas J TJ; Theusch, Elizabeth E; Haldar, Tanushree T; Ranatunga, Dilrini K DK; Jorgenson, Eric E; Medina, Marisa W MW; Kvale, Mark N MN; Kwok, Pui-Yan PY; Schaefer, Catherine C; Krauss, Ronald M RM; Iribarren, Carlos C; Risch, Neil N
Publication Date: 2018-03

Variant appearance in text: rs17660708
PubMed Link: 29507422
Variant Present in the following documents:
  • Main text
  • NIHMS936300-supplement-3.pdf
View BVdb publication page