rs4705862
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4705862(A;A) |
Make rs4705862(A;T) |
Make rs4705862(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 132477527 |
is a | snp |
is | mentioned by |
dbSNP | rs4705862 |
dbSNP (classic) | rs4705862 |
ClinGen | rs4705862 |
ebi | rs4705862 |
HLI | rs4705862 |
Exac | rs4705862 |
Gnomad | rs4705862 |
Varsome | rs4705862 |
LitVar | rs4705862 |
Map | rs4705862 |
PheGenI | rs4705862 |
Biobank | rs4705862 |
1000 genomes | rs4705862 |
hgdp | rs4705862 |
ensembl | rs4705862 |
geneview | rs4705862 |
scholar | rs4705862 |
rs4705862 | |
pharmgkb | rs4705862 |
gwascentral | rs4705862 |
openSNP | rs4705862 |
23andMe | rs4705862 |
SNPshot | rs4705862 |
SNPdbe | rs4705862 |
MSV3d | rs4705862 |
GWAS Ctlg | rs4705862 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 25833190] Disease-associated SNPs From non-coding regions in juvenile idiopathic arthritis are located within or adjacent to functional genomic elements of human neutrophils and CD4+ T Cells