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PIWIL2 c.1989+274A>G
Variant ID: 8-22169087-A-G
NM_018068.3(
PIWIL2
):c.1989+274A>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A Key GWAS-Identified Genetic Variant Contributes to Hyperlipidemia by Upregulating miR-320a.
Iscience
Yin, Zhongwei Z; Zhao, Yanru Y; Du, Hengzhi H; Nie, Xiang X; Li, Huaping H; Fan, Jiahui J; He, Mengying M; Dai, Beibei B; Zhang, Xudong X; Yuan, Shuai S; Wen, Zheng Z; Chen, Chen C; Wang, Dao Wen DW
Publication Date: 2020-12-18
Variant appearance in text: rs4266653
PubMed Link:
33294796
Variant Present in the following documents:
main.pdf
mmc1.pdf
View BVdb publication page
Pharmacogenomics of Cognitive Dysfunction and Neuropsychiatric Disorders in Dementia.
International Journal Of Molecular Sciences
Cacabelos, Ramon R
Publication Date: 2020-04-26
Variant appearance in text: rs4266653
PubMed Link:
32357528
Variant Present in the following documents:
Main text
ijms-21-03059.pdf
View BVdb publication page
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.
Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018
Variant appearance in text: PIWIL2: 1989+274A>G; rs4266653
PubMed Link:
30319441
Variant Present in the following documents:
Table_5.xlsx, sheet 1
Table_6.xlsx, sheet 1
View BVdb publication page