SATB2 c.1740+15888A>C

Variant ID: 2-200157595-T-G

NM_001172509.1(SATB2):c.1740+15888A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Carter, Tonia C TC; Molloy, Anne M AM; Pangilinan, Faith F; Troendle, James F JF; Kirke, Peadar N PN; Conley, Mary R MR; Orr, David J A DJ; Earley, Michael M; McKiernan, Eamon E; Lynn, Ena C EC; Doyle, Anne A; Scott, John M JM; Brody, Lawrence C LC; Mills, James L JL
Publication Date: 2010-02

Variant appearance in text: rs1446636
PubMed Link: 19937600
Variant Present in the following documents:
  • Main text
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