GGT7 c.744-70C>T

Variant ID: 20-33447915-G-A

NM_178026.2(GGT7):c.744-70C>T

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Genetically predicted testosterone and cancers risk in men: a two-sample Mendelian randomization study.

Journal Of Translational Medicine
Chang, Junke J; Wu, Yongming Y; Zhou, Sicheng S; Tian, Ye Y; Wang, Yan Y; Tian, Jie J; Song, Wenpeng W; Dong, Yinxian Y; Li, Jue J; Zhao, Ziyi Z; Che, Guowei G
Publication Date: 2022-12-08

Variant appearance in text: rs2295094
PubMed Link: 36482455
Variant Present in the following documents:
  • Main text
  • 12967_2022_Article_3783.pdf
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs2295094
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: GGT7: 744-70C>T; rs2295094
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
View BVdb publication page



Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications
Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S
Publication Date: 2018-03-02

Variant appearance in text: rs2295094
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2295094
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page