rs3088362
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3088362(A;A) |
Make rs3088362(A;C) |
Make rs3088362(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 43859494 |
Gene | CCDC122 |
is a | snp |
is | mentioned by |
dbSNP | rs3088362 |
dbSNP (classic) | rs3088362 |
ClinGen | rs3088362 |
ebi | rs3088362 |
HLI | rs3088362 |
Exac | rs3088362 |
Gnomad | rs3088362 |
Varsome | rs3088362 |
LitVar | rs3088362 |
Map | rs3088362 |
PheGenI | rs3088362 |
Biobank | rs3088362 |
1000 genomes | rs3088362 |
hgdp | rs3088362 |
ensembl | rs3088362 |
geneview | rs3088362 |
scholar | rs3088362 |
rs3088362 | |
pharmgkb | rs3088362 |
gwascentral | rs3088362 |
openSNP | rs3088362 |
23andMe | rs3088362 |
SNPshot | rs3088362 |
SNPdbe | rs3088362 |
MSV3d | rs3088362 |
GWAS Ctlg | rs3088362 |
GMAF | 0.2034 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
Variant in the CCDC122 region associated with increased susceptibility to leprosy in Asians, according to the 23andMe blog 23andMe's blog. The risk allele is A, and the odds ratio is 1.52.