RESULT OF MUTATION
Total records: 1 Records
 
Record No:1
| ACCESS NO | 301016 | 
| GENE_NAME | ORMDL3 | 
| dbSNP_ID | rs7216389 | 
| CHANGES | C/T | 
| ANCESTRAL_ALLELES | T | 
| FUNCTIONAL_CONSEQUENCES | Intron Variant | 
| DISEASE | Asthma | 
| POPULATION | - | 
| PMID | 26064206 | 
| COMMENTS | rs7216389 was significantly associated with increased asthma risk in overall population. Children with variant T allele (TT or TC) and adults with TT homozygote in rs7216389 are at high risks to suffer from asthma. |