Annotation Detail
Information
- Associated Genes
- ALOX12
- Associated Variants
-
rs6502997
rs6502998
ALOX12 p.Asn322Ser (p.N322S) ( ENST00000251535.11 )
ALOX12 p.Leu634= (p.L634=) ( ENST00000251535.11 )
rs6502997
rs6502998
ALOX12 p.Asn322Ser (p.N322S) ( ENST00000251535.11 )
ALOX12 p.Leu634= (p.L634=) ( ENST00000251535.11 ) - Associated Disease
- Toxoplasmosis, Congenital
- Source Database
- DisGeNET
- Description
- Here we report that the human ALOX12 gene has susceptibility alleles for human congenital toxoplasmosis (rs6502997 [P, <0.000309], rs312462 [P, <0.028499], rs6502998 [P, <0.029794], and rs434473 [P, <0.038516]).
- Pubmed
- 24686056
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2014
Drugs