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SIGLEC5 c.1464+2151G>A
Variant ID: 19-52127134-C-T
NM_003830.3(
SIGLEC5
):c.1464+2151G>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:
Genetic susceptibility of common polymorphisms in NIN and SIGLEC5 to chronic periodontitis.
Scientific Reports
Tong, Hua H; Wei, Zhuliang Z; Yin, Jing J; Zhang, Bo B; Zhang, Tianxiao T; Deng, Chunni C; Huang, Yali Y; Zhang, Nan N
Publication Date: 2019-02-14
Variant appearance in text: rs4802831
PubMed Link:
30765789
Variant Present in the following documents:
Main text
41598_2019_Article_38632.pdf
View BVdb publication page
Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence.
Plos One
Johnson, Catherine C; Drgon, Tomas T; Walther, Donna D; Uhl, George R GR
Publication Date: 2011
Variant appearance in text: rs4802831
PubMed Link:
21818250
Variant Present in the following documents:
Main text
View BVdb publication page