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TNFSF8 c.310+665A>G
Variant ID: 9-117667443-T-C
NM_001244.3(
TNFSF8
):c.310+665A>G
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 between TNFSF4, TNFSF8 and TNFSF15 and Behçet's disease but not VKH syndrome in Han Chinese.
Oncotarget
Jiang, Yan Y; Cheng, Ling L; Li, Xin X; Zhou, Wenke W; Zhang, Li L
Publication Date: 2017-12-01
Variant appearance in text: rs3181362
PubMed Link:
29285231
Variant Present in the following documents:
Main text
oncotarget-08-105037.pdf
View BVdb publication page
Genome-wide SNP typing reveals signatures of population history.
Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07
Variant appearance in text: rs3181362
PubMed Link:
18485661
Variant Present in the following documents:
Main text
View BVdb publication page