RERE c.1204-1956T>A

Variant ID: 1-8484823-A-T

NM_001042681.1(RERE):c.1204-1956T>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


A comprehensive meta-analysis and prioritization study to identify vitiligo associated coding and non-coding SNV candidates using web-based bioinformatics tools.

Scientific Reports
Dutta, Tithi T; Mitra, Sayantan S; Saha, Arpan A; Ganguly, Kausik K; Pyne, Tushar T; Sengupta, Mainak M
Publication Date: 2022-08-25

Variant appearance in text: rs301807
PubMed Link: 36008553
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_18766.pdf
View BVdb publication page



Smoking and heart failure: a Mendelian randomization and mediation analysis.

Esc Heart Failure
Lu, Yunlong Y; Xu, Zhouming Z; Georgakis, Marios K MK; Wang, Zhen Z; Lin, Hefeng H; Zheng, Liangrong L
Publication Date: 2021-06

Variant appearance in text: rs301807
PubMed Link: 33656795
Variant Present in the following documents:
  • EHF2-8-1954-s001.pdf
View BVdb publication page



Genetic loci shared between major depression and intelligence with mixed directions of effect.

Nature Human Behaviour
Bahrami, Shahram S; Shadrin, Alexey A; Frei, Oleksandr O; O'Connell, Kevin S KS; Bettella, Francesco F; Krull, Florian F; Fan, Chun C CC; Røssberg, Jan I JI; Hindley, Guy G; Ueland, Torill T; Dale, Anders M AM; Djurovic, Srdjan S; Steen, Nils Eiel NE; Smeland, Olav B OB; Andreassen, Ole A OA
Publication Date: 2021-06

Variant appearance in text: rs301807
PubMed Link: 33462475
Variant Present in the following documents:
  • Main text
  • nihms-1652425.pdf
  • NIHMS1652425-supplement-1.pdf
View BVdb publication page



Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population.

Frontiers In Genetics
Cheng, Lu L; Liang, Bo B; Tang, Xian-Fa XF; Cai, Xin-Ying XY; Cheng, Hui H; Zheng, Xiao-Dong XD; Zheng, Jie J; Wang, Meng-Wei MW; Zhu, Jun J; Zhou, Fu-Sheng FS; Li, Pan P; Xiao, Feng-Li FL
Publication Date: 2020

Variant appearance in text: rs301807
PubMed Link: 33343616
Variant Present in the following documents:
  • Main text
  • fgene-11-542275.pdf
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs301807
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Early-onset autoimmune vitiligo associated with an enhancer variant haplotype that upregulates class II HLA expression.

Nature Communications
Jin, Ying Y; Roberts, Genevieve H L GHL; Ferrara, Tracey M TM; Ben, Songtao S; van Geel, Nanja N; Wolkerstorfer, Albert A; Ezzedine, Khaled K; Siebert, Janet J; Neff, Charles P CP; Palmer, Brent E BE; Santorico, Stephanie A SA; Spritz, Richard A RA
Publication Date: 2019-01-23

Variant appearance in text: rs301807
PubMed Link: 30674883
Variant Present in the following documents:
  • 41467_2019_8337_MOESM1_ESM.pdf
View BVdb publication page