G2Cdb::Allele report
- Mutation type
- SNP
Altered genes (1)
Gene |
Symbol |
Species |
Description |
G00002098 |
GRIN1 |
Homo sapiens |
glutamate receptor, ionotropic, N-methyl D-aspartate 1 |
Diseases (1)
Disease |
Description |
Nervous effect |
D00000162 |
Alcoholism |
Y |
Literature (1)
Pubmed - other