SMARCA4 c.-32+760G>T

Variant ID: 19-11072610-G-T

NM_003072.5(SMARCA4):c.-32+760G>T

This variant was identified in 10 publications

View GRCh38 version.




Publications:


Identification of methylation changes associated with positive and negative growth deviance in Gambian infants using a targeted methyl sequencing approach of genomic DNA.

Faseb Bioadvances
Quilter, Claire R CR; Harvey, Kerry M KM; Bauer, Julien J; Skinner, Benjamin M BM; Gomez, Maria M; Shrivastava, Manu M; Doel, Andrew M AM; Drammeh, Saikou S; Dunger, David B DB; Moore, Sophie E SE; Ong, Ken K KK; Prentice, Andrew M AM; Bernstein, Robin M RM; Sargent, Carole A CA; Affara, Nabeel A NA
Publication Date: 2021-04

Variant appearance in text: rs11879293
PubMed Link: 33842847
Variant Present in the following documents:
  • FBA2-3-205-s004.xlsx, sheet 3
View BVdb publication page



The roles of mutated SWI/SNF complexes in the initiation and development of hepatocellular carcinoma and its regulatory effect on the immune system: A review.

Cell Proliferation
Hu, Bo B; Lin, Jian-Zhen JZ; Yang, Xiao-Bo XB; Sang, Xin-Ting XT
Publication Date: 2020-04

Variant appearance in text: rs11879293
PubMed Link: 32162380
Variant Present in the following documents:
  • Main text
View BVdb publication page



Oncogene-dependent function of BRG1 in hepatocarcinogenesis.

Cell Death & Disease
Wang, Pan P; Song, Xinhua X; Cao, Dan D; Cui, Kairong K; Wang, Jingxiao J; Utpatel, Kirsten K; Shang, Runze R; Wang, Haichuan H; Che, Li L; Evert, Matthias M; Zhao, Keji K; Calvisi, Diego F DF; Chen, Xin X
Publication Date: 2020-02-04

Variant appearance in text: rs11879293
PubMed Link: 32019910
Variant Present in the following documents:
  • Main text
  • 41419_2020_Article_2289.pdf
View BVdb publication page



The genetic polymorphisms of ZC3HC1 and SMARCA4 are associated with hypertension risk.

Molecular Genetics & Genomic Medicine
Ma, Huijun H; He, Yongjun Y; Bai, Mei M; Zhu, Linhao L; He, Xue X; Wang, Li L; Jin, Tianbo T
Publication Date: 2019-11

Variant appearance in text: rs11879293
PubMed Link: 31507094
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sex-specific association of SH2B3 and SMARCA4 polymorphisms with coronary artery disease susceptibility.

Oncotarget
Ji, Yuqiang Y; Song, Yanbin Y; Wang, Qingwen Q; Xu, Pengcheng P; Zhao, Zhao Z; Li, Xia X; Wang, Nan N; Jin, Tianbo T; Chen, Chao C
Publication Date: 2017-08-29

Variant appearance in text: rs11879293
PubMed Link: 28938645
Variant Present in the following documents:
  • Main text
  • oncotarget-08-59397.pdf
View BVdb publication page



Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs11879293
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



Variants in the SMARCA4 gene was associated with coronary heart disease susceptibility in Chinese han population.

Oncotarget
Guo, Xuan X; Wang, Xiaohong X; Wang, Yuan Y; Zhang, Chunyan C; Quan, Xiaohui X; Zhang, Yan Y; Jia, Shan S; Ma, Weidong W; Fan, Yajie Y; Wang, Congxia C
Publication Date: 2017-01-31

Variant appearance in text: rs11879293
PubMed Link: 28055962
Variant Present in the following documents:
  • Main text
  • oncotarget-08-7350.pdf
View BVdb publication page



CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.

Journal Of Neuro-Oncology
Dahlin, Anna M AM; Hollegaard, Mads V MV; Wibom, Carl C; Andersson, Ulrika U; Hougaard, David M DM; Deltour, Isabelle I; Hjalmars, Ulf U; Melin, Beatrice B
Publication Date: 2015-10

Variant appearance in text: rs11879293
PubMed Link: 26290144
Variant Present in the following documents:
  • 11060_2015_1891_MOESM1_ESM.pdf
View BVdb publication page



Genetic variant in SWI/SNF complexes influences hepatocellular carcinoma risk: a new clue for the contribution of chromatin remodeling in carcinogenesis.

Scientific Reports
Zhong, Rong R; Liu, Li L; Tian, Yao Y; Wang, Ying Y; Tian, Jing J; Zhu, Bei-bei BB; Chen, Wei W; Qian, Jia-ming JM; Zou, Li L; Xiao, Min M; Shen, Na N; Yang, Hong H; Lou, Jiao J; Qiu, Qian Q; Ke, Jun-tao JT; Lu, Xing-hua XH; Wang, Zhen-ling ZL; Song, Wei W; Zhang, Ti T; Li, Hui H; Wang, Li L; Miao, Xiao-ping XP
Publication Date: 2014-02-21

Variant appearance in text: rs11879293
PubMed Link: 24556940
Variant Present in the following documents:
  • Main text
View BVdb publication page



Targeted re-sequencing identified rs3106189 at the 5' UTR of TAPBP and rs1052918 at the 3' UTR of TCF3 to be associated with the overall survival of colorectal cancer patients.

Plos One
Shao, Jiaofang J; Lou, Xiaoyan X; Wang, Jun J; Zhang, Jing J; Chen, Chen C; Hua, Dasong D; Mo, Fan F; Han, Xu X; Zheng, Shu S; Lin, Biaoyang B
Publication Date: 2013

Variant appearance in text: rs11879293
PubMed Link: 23940558
Variant Present in the following documents:
  • pone.0070307.s002.xlsx, sheet 1
View BVdb publication page