MYL2 c.169+671T>G

Variant ID: 12-111352848-A-C

NM_000432.3(MYL2):c.169+671T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.

Bmc Medical Genetics
Levy, Daniel D; Larson, Martin G MG; Benjamin, Emelia J EJ; Newton-Cheh, Christopher C; Wang, Thomas J TJ; Hwang, Shih-Jen SJ; Vasan, Ramachandran S RS; Mitchell, Gary F GF
Publication Date: 2007-09-19

Variant appearance in text: rs933296
PubMed Link: 17903302
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S3.pdf
View BVdb publication page