WNT3A c.314-13533A>G

Variant ID: 1-228224824-A-G

NM_033131.3(WNT3A):c.314-13533A>G

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Clinical relevance of genetic polymorphisms in WNT signaling pathway (SFRP1, WNT3A, CTNNB1, WIF-1, DKK-1, LRP5, LRP6) on pulmonary tuberculosis in a Chinese population.

Frontiers In Immunology
Huang, Qian Q; Wang, Chao-Cai CC; Liu, Yun-Guang YG; Zhao, Chang-Ming CM; Zhang, Tian-Ping TP; Liu, Yan Y; Wang, Hua H
Publication Date: 2022

Variant appearance in text: rs3121310
PubMed Link: 36569862
Variant Present in the following documents:
  • Main text
  • fimmu-13-1011700.pdf
View BVdb publication page



WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases.

Frontiers In Cardiovascular Medicine
Ren, Huan H; Luo, Jian-Quan JQ; Ouyang, Fan F; Cheng, Li L; Chen, Xiao-Ping XP; Zhou, Hong-Hao HH; Huang, Wei-Hua WH; Zhang, Wei W
Publication Date: 2021

Variant appearance in text: rs3121310
PubMed Link: 34322525
Variant Present in the following documents:
  • Main text
  • fcvm-08-675222.pdf
View BVdb publication page



MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.

Bmc Medical Genomics
Suzuki, Akiko A; Li, Aimin A; Gajera, Mona M; Abdallah, Nada N; Zhang, Musi M; Zhao, Zhongming Z; Iwata, Junichi J
Publication Date: 2019-07-01

Variant appearance in text: rs3121310
PubMed Link: 31262291
Variant Present in the following documents:
  • 12920_2019_546_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Association of the WNT3 Variations and the Risk of Non-Syndromic Cleft Lip and Palate in a Population of Iranian Infants.

Avicenna Journal Of Medical Biotechnology
Farrokhi Karibozorg, Homa H; Masoudian, Nahid N; Saliminejad, Kioomars K; Ebadifar, Asghar A; Kamali, Koorosh K; Khorram Khorshid, Hamid Reza HR
Publication Date: 2018

Variant appearance in text: rs3121310
PubMed Link: 30090211
Variant Present in the following documents:
  • Main text
  • AJMB-10-168.pdf
View BVdb publication page



Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal
Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X
Publication Date: 2014-12

Variant appearance in text: rs3121310
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page



WNT3A gene polymorphisms are associated with bone mineral density variation in postmenopausal mestizo women of an urban Mexican population: findings of a pathway-based high-density single nucleotide screening.

Age (Dordrecht, Netherlands)
Velázquez-Cruz, Rafael R; García-Ortiz, Humberto H; Castillejos-López, Manuel M; Quiterio, Manuel M; Valdés-Flores, Margarita M; Orozco, Lorena L; Villarreal-Molina, Teresa T; Salmerón, Jorge J
Publication Date: 2014-06

Variant appearance in text: rs3121310
PubMed Link: 24584697
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: rs3121310
PubMed Link: 18413325
Variant Present in the following documents:
  • Main text
View BVdb publication page