Bibliome.ai browser hg19
Search
About
Stats
FAQ
SLC2A3 c.108+323G>A
Variant ID: 12-8086083-C-T
NM_006931.2(
SLC2A3
):c.108+323G>A
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:
Associations of cognitive impairment in patients with schizophrenia with genetic features and with schizophrenia-related structural and functional brain changes.
Frontiers In Genetics
Zhuo, Chuanjun C; Tian, Hongjun H; Chen, Jiayue J; Li, Qianchen Q; Yang, Lei L; Zhang, Qiuyu Q; Chen, Guangdong G; Cheng, Langlang L; Zhou, Chunhua C; Song, Xueqin X
Publication Date: 2022
Variant appearance in text: rs7976243
PubMed Link:
36061201
Variant Present in the following documents:
Main text
fgene-13-880027.pdf
View BVdb publication page
Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis.
Plos One
Aterido, AdriĆ A; Palacio, Carlos C; Marsal, Sara S; Avila, Gabriela G; JuliĆ , Antonio A
Publication Date: 2014
Variant appearance in text: rs7976243
PubMed Link:
24959711
Variant Present in the following documents:
Main text
pone.0100690.pdf
View BVdb publication page