KLF16 c.*1876T>C

Variant ID: 19-1852582-A-G

NM_031918.3(KLF16):c.*1876T>C

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Reconstructing SNP allele and genotype frequencies from GWAS summary statistics.

Scientific Reports
Yang, Zhiyu Z; Paschou, Peristera P; Drineas, Petros P
Publication Date: 2022-05-17

Variant appearance in text: rs1054972
PubMed Link: 35581276
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_12185.pdf
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Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.

Nature Genetics
Peyrot, Wouter J WJ; Price, Alkes L AL
Publication Date: 2021-04

Variant appearance in text: rs1054972
PubMed Link: 33686288
Variant Present in the following documents:
  • Main text
  • nihms-1663271.pdf
View BVdb publication page



Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.

Molecular Psychiatry
Byrne, Enda M EM; Zhu, Zhihong Z; Qi, Ting T; Skene, Nathan G NG; Bryois, Julien J; Pardinas, Antonio F AF; Stahl, Eli E; Smoller, Jordan W JW; Rietschel, Marcella M; , ; , ; Owen, Michael J MJ; Walters, James T R JTR; O'Donovan, Michael C MC; McGrath, John G JG; Hjerling-Leffler, Jens J; Sullivan, Patrick F PF; Goddard, Michael E ME; Visscher, Peter M PM; Yang, Jian J; Wray, Naomi R NR
Publication Date: 2021-06

Variant appearance in text: rs1054972
PubMed Link: 32398722
Variant Present in the following documents:
  • Main text
View BVdb publication page



Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.

Molecular Psychiatry
Byrne, Enda M EM; Zhu, Zhihong Z; Qi, Ting T; Skene, Nathan G NG; Bryois, Julien J; Pardinas, Antonio F AF; Stahl, Eli E; Smoller, Jordan W JW; Rietschel, Marcella M; , ; , ; Owen, Michael J MJ; Walters, James T R JTR; O'Donovan, Michael C MC; McGrath, John G JG; Hjerling-Leffler, Jens J; Sullivan, Patrick F PF; Goddard, Michael E ME; Visscher, Peter M PM; Yang, Jian J; Wray, Naomi R NR
Publication Date: 2021-06

Variant appearance in text: rs1054972
PubMed Link: 32398722
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs1054972
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page