NSF c.1908+9443A>G

Variant ID: 17-44815743-A-G

NM_006178.3(NSF):c.1908+9443A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association of the WNT3 polymorphisms and non-syndromic cleft lip with or without cleft palate: evidence from a meta-analysis.

Bioscience Reports
Wang, Bing-Qian BQ; Gao, Shu-Tao ST; Chen, Kun K; Xu, Zhu-Qiu ZQ; Sun, Jia-Ming JM; Xia, Yun Y; Lv, Zheng-Tao ZT
Publication Date: 2018-12-21

Variant appearance in text: rs7216231
PubMed Link: 30355643
Variant Present in the following documents:
  • Main text
  • bsr-38-bsr20181676.pdf
View BVdb publication page



Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Letra, Ariadne A; Maili, Lorena L; Mulliken, John B JB; Buchanan, Edward E; Blanton, Susan H SH; Hecht, Jacqueline T JT
Publication Date: 2014-09

Variant appearance in text: rs7216231
PubMed Link: 25163644
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.

Human Molecular Genetics
Chiquet, Brett T BT; Blanton, Susan H SH; Burt, Amber A; Ma, Deqiong D; Stal, Samuel S; Mulliken, John B JB; Hecht, Jacqueline T JT
Publication Date: 2008-07-15

Variant appearance in text: rs7216231
PubMed Link: 18413325
Variant Present in the following documents:
  • Main text
View BVdb publication page