MLXIPL c.1671+32T>C

Variant ID: 7-73011163-A-G

NM_032951.2(MLXIPL):c.1671+32T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.

Molecular Genetics & Genomic Medicine
Kopp, Nathan D ND; Parrish, Phoebe C R PCR; Lugo, Michael M; Dougherty, Joseph D JD; Kozel, Beth A BA
Publication Date: 2018-09

Variant appearance in text: rs782188633
PubMed Link: 30008175
Variant Present in the following documents:
  • MGG3-6-749-s003.xlsx, sheet 1
View BVdb publication page