RFX6 c.672+1985G>A

Variant ID: 6-117218355-G-A

NM_173560.3(RFX6):c.672+1985G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Puffenberger, Erik G EG; Hu-Lince, Diane D; Parod, Jennifer M JM; Craig, David W DW; Dobrin, Seth E SE; Conway, Andrew R AR; Donarum, Elizabeth A EA; Strauss, Kevin A KA; Dunckley, Travis T; Cardenas, Javier F JF; Melmed, Kara R KR; Wright, Courtney A CA; Liang, Winnie W; Stafford, Phillip P; Flynn, C Robert CR; Morton, D Holmes DH; Stephan, Dietrich A DA
Publication Date: 2004-08-10

Variant appearance in text: rs1321370
PubMed Link: 15273283
Variant Present in the following documents:
  • Main text
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