ABCA1 c.-93+3112G>T

Variant ID: 9-107687104-C-A

NM_005502.4(ABCA1):c.-93+3112G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide allele and haplotype-sharing patterns suggested one unique Hmong-Mein-related lineage and biological adaptation history in Southwest China.

Human Genomics
Wang, Jiawen J; Yang, Lin L; Duan, Shuhan S; Sun, Qiuxia Q; Li, Youjing Y; Wu, Jun J; Wu, Wenxin W; Wang, Zheng Z; Liu, Yan Y; Tang, Renkuan R; Yang, Junbao J; Liu, Chao C; Yuan, Buhong B; Wang, Daoyong D; Xu, Jianwei J; Wang, Mengge M; He, Guanglin G
Publication Date: 2023-01-31

Variant appearance in text: rs2472377
PubMed Link: 36721228
Variant Present in the following documents:
  • Main text
  • 40246_2023_Article_452.pdf
View BVdb publication page



3'UTR Polymorphism in ACSL1 Gene Correlates with Expression Levels and Poor Clinical Outcome in Colon Cancer Patients.

Plos One
Vargas, Teodoro T; Moreno-Rubio, Juan J; Herranz, Jesús J; Cejas, Paloma P; Molina, Susana S; Mendiola, Marta M; Burgos, Emilio E; Custodio, Ana B AB; De Miguel, María M; Martín-Hernández, Roberto R; Reglero, Guillermo G; Feliu, Jaime J; Ramírez de Molina, Ana A
Publication Date: 2016

Variant appearance in text: rs2472377
PubMed Link: 27992526
Variant Present in the following documents:
  • Main text
  • pone.0168423.pdf
View BVdb publication page