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VRK2 c.1183-2664C>T
Variant ID: 2-58383820-C-T
NM_006296.6(
VRK2
):c.1183-2664C>T
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Identification of a Risk Locus at 7p22.3 for Schizophrenia and Bipolar Disorder in East Asian Populations.
Frontiers In Genetics
Li, Wenqiang W; Zhang, Chu-Yi CY; Liu, Jiewei J; Guan, Fanglin F; Shao, Minglong M; Zhang, Luwen L; Liu, Qing Q; Yang, Yongfeng Y; Su, Xi X; Zhang, Yan Y; Xiao, Xiao X; Luo, Xiong-Jian XJ; Li, Ming M; Lv, Luxian L
Publication Date: 2021
Variant appearance in text: rs7596038
PubMed Link:
34976021
Variant Present in the following documents:
Main text
fgene-12-789512.pdf
View BVdb publication page
VRK2, a Candidate Gene for Psychiatric and Neurological Disorders.
Molecular Neuropsychiatry
Li, Ming M; Yue, Weihua W
Publication Date: 2018-12
Variant appearance in text: rs7596038
PubMed Link:
30643786
Variant Present in the following documents:
Main text
View BVdb publication page