rs998592
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs998592(A;A) |
Make rs998592(A;G) |
Make rs998592(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 11105821 |
Gene | CLEC16A |
is a | snp |
is | mentioned by |
dbSNP | rs998592 |
dbSNP (classic) | rs998592 |
ClinGen | rs998592 |
ebi | rs998592 |
HLI | rs998592 |
Exac | rs998592 |
Gnomad | rs998592 |
Varsome | rs998592 |
LitVar | rs998592 |
Map | rs998592 |
PheGenI | rs998592 |
Biobank | rs998592 |
1000 genomes | rs998592 |
hgdp | rs998592 |
ensembl | rs998592 |
geneview | rs998592 |
scholar | rs998592 |
rs998592 | |
pharmgkb | rs998592 |
gwascentral | rs998592 |
openSNP | rs998592 |
23andMe | rs998592 |
SNPshot | rs998592 |
SNPdbe | rs998592 |
MSV3d | rs998592 |
GWAS Ctlg | rs998592 |
GMAF | 0.348 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20849399] More CLEC16A gene variants associated with multiple sclerosis
[PMID 22534877] Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance