NOS1AP c.177+22443G>A

Variant ID: 1-162146709-G-A

NM_014697.2(NOS1AP):c.177+22443G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Impact of ancestry and common genetic variants on QT interval in African Americans.

Circulation. Cardiovascular Genetics
Smith, J Gustav JG; Avery, Christy L CL; Evans, Daniel S DS; Nalls, Michael A MA; Meng, Yan A YA; Smith, Erin N EN; Palmer, Cameron C; Tanaka, Toshiko T; Mehra, Reena R; Butler, Anne M AM; Young, Taylor T; Buxbaum, Sarah G SG; Kerr, Kathleen F KF; Berenson, Gerald S GS; Schnabel, Renate B RB; Li, Guo G; Ellinor, Patrick T PT; Magnani, Jared W JW; Chen, Wei W; Bis, Joshua C JC; Curb, J David JD; Hsueh, Wen-Chi WC; Rotter, Jerome I JI; Liu, Yongmei Y; Newman, Anne B AB; Limacher, Marian C MC; North, Kari E KE; Reiner, Alexander P AP; Quibrera, P Miguel PM; Schork, Nicholas J NJ; Singleton, Andrew B AB; Psaty, Bruce M BM; Soliman, Elsayed Z EZ; Solomon, Allen J AJ; Srinivasan, Sathanur R SR; Alonso, Alvaro A; Wallace, Robert R; Redline, Susan S; Zhang, Zhu-Ming ZM; Post, Wendy S WS; Zonderman, Alan B AB; Taylor, Herman A HA; Murray, Sarah S SS; Ferrucci, Luigi L; Arking, Dan E DE; Evans, Michele K MK; Fox, Ervin R ER; Sotoodehnia, Nona N; Heckbert, Susan R SR; Whitsel, Eric A EA; Newton-Cheh, Christopher C; ,
Publication Date: 2012-12

Variant appearance in text: rs7534004
PubMed Link: 23166209
Variant Present in the following documents:
  • Main text
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