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. |