MRVI1 c.226-3117T>C

Variant ID: 11-10658735-A-G

NM_130385.3(MRVI1):c.226-3117T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


STEPS: an efficient prospective likelihood approach to genetic association analyses of secondary traits in extreme phenotype sequencing.

Biostatistics (Oxford, England)
Bi, Wenjian W; Li, Yun Y; Smeltzer, Matthew P MP; Gao, Guimin G; Zhao, Shengli S; Kang, Guolian G
Publication Date: 2020-01-01

Variant appearance in text: rs1035691
PubMed Link: 30007308
Variant Present in the following documents:
  • Main text
View BVdb publication page