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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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