rs34826052
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs34826052(G;T) |
Make rs34826052(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 35345697 |
Gene | CD22, MIR5196 |
is a | snp |
is | mentioned by |
dbSNP | rs34826052 |
dbSNP (classic) | rs34826052 |
ClinGen | rs34826052 |
ebi | rs34826052 |
HLI | rs34826052 |
Exac | rs34826052 |
Gnomad | rs34826052 |
Varsome | rs34826052 |
LitVar | rs34826052 |
Map | rs34826052 |
PheGenI | rs34826052 |
Biobank | rs34826052 |
1000 genomes | rs34826052 |
hgdp | rs34826052 |
ensembl | rs34826052 |
geneview | rs34826052 |
scholar | rs34826052 |
rs34826052 | |
pharmgkb | rs34826052 |
gwascentral | rs34826052 |
openSNP | rs34826052 |
23andMe | rs34826052 |
SNPshot | rs34826052 |
SNPdbe | rs34826052 |
MSV3d | rs34826052 |
GWAS Ctlg | rs34826052 |
GMAF | 0.05601 |
Max Magnitude | 0 |
[PMID 21961844] Association study of B-cell marker gene polymorphisms in European Caucasian patients with systemic sclerosis
[PMID 21247474] Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19.