RUNX2 c.1021+16312C>T

Variant ID: 6-45496456-C-T

NM_001024630.3(RUNX2):c.1021+16312C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.

Genetic Epidemiology
Sull, Jae Woong JW; Liang, Kung-Yee KY; Hetmanski, Jacqueline B JB; Fallin, Margaret Daniele MD; Ingersoll, Roxann G RG; Park, Jiwan J; Wu-Chou, Yah-Huei YH; Chen, Philip K PK; Chong, Samuel S SS; Cheah, Felicia F; Yeow, Vincent V; Park, Beyoung Yun BY; Jee, Sun Ha SH; Jabs, Ethylin Wang EW; Redett, Richard R; Jung, Euiju E; Ruczinski, Ingo I; Scott, Alan F AF; Beaty, Terri H TH
Publication Date: 2008-09

Variant appearance in text: rs13207392
PubMed Link: 18357615
Variant Present in the following documents:
  • Main text
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