CSMD1 c.819-62881T>C

Variant ID: 8-3674445-A-G

NM_033225.5(CSMD1):c.819-62881T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the Multi-Ethnic Study of Atherosclerosis.

Bmc Genetics
Ware, Erin B EB; Mukherjee, Bhramar B; Sun, Yan V YV; Diez-Roux, Ana V AV; Kardia, Sharon L R SL; Smith, Jennifer A JA
Publication Date: 2015-10-12

Variant appearance in text: rs17067630
PubMed Link: 26459564
Variant Present in the following documents:
  • Main text
  • 12863_2015_Article_274.pdf
View BVdb publication page