MPHOSPH9 c.1087+1760A>T

Variant ID: 12-123697531-T-A

NM_022782.3(MPHOSPH9):c.1087+1760A>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exploring Potential Causal Genes for Uterine Leiomyomas: A Summary Data-Based Mendelian Randomization and FUMA Analysis.

Frontiers In Genetics
Dai, Yuxin Y; Liu, Xudong X; Zhu, Yining Y; Mao, Su S; Yang, Jingyun J; Zhu, Lan L
Publication Date: 2022

Variant appearance in text: rs10772996
PubMed Link: 35903355
Variant Present in the following documents:
  • Main text
  • fgene-13-890007.pdf
View BVdb publication page