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. |