rs10208769
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10208769(A;A) |
Make rs10208769(A;T) |
Make rs10208769(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 61378479 |
Gene | USP34 |
is a | snp |
is | mentioned by |
dbSNP | rs10208769 |
dbSNP (classic) | rs10208769 |
ClinGen | rs10208769 |
ebi | rs10208769 |
HLI | rs10208769 |
Exac | rs10208769 |
Gnomad | rs10208769 |
Varsome | rs10208769 |
LitVar | rs10208769 |
Map | rs10208769 |
PheGenI | rs10208769 |
Biobank | rs10208769 |
1000 genomes | rs10208769 |
hgdp | rs10208769 |
ensembl | rs10208769 |
geneview | rs10208769 |
scholar | rs10208769 |
rs10208769 | |
pharmgkb | rs10208769 |
gwascentral | rs10208769 |
openSNP | rs10208769 |
23andMe | rs10208769 |
SNPshot | rs10208769 |
SNPdbe | rs10208769 |
MSV3d | rs10208769 |
GWAS Ctlg | rs10208769 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 28493913] Pathogenic variants screening in seventeen candidate genes on 2p15 for association with ankylosing spondylitis in a Han Chinese population.