Table 4 The SNPs in significant triplets in ADNI dataset mapped to a gene associated with a disease
rsID | Chr | Pos | Gene | Phenotype |
|---|---|---|---|---|
rs7157639 | 14 | 53,388,161 | FERMT2 | Alzheimer Disease/Hereditary Spastic Paraplegia |
rs9366664 | 6 | 10,892,499 | SYCP2L | Age-related hearing impairment |
rs10017010 | 4 | 25,188,718 | SEPSECS | Pontocerebellar hypoplasia type 2es |
rs2207851 | 6 | 144,337,886 | PLAGL1 | Transient neonatal diabetes mellitus / Paternal uniparental disomy of chromosome 6 |
rs2824808 | 21 | 19,775,220 | TMPRSS15 | Enterokinase deficiency |
rs324389 | 7 | 34,777,714 | NPSR1 | Asthma-Related Traits |
rs3780792 | 9 | 136,835,343 | VAV2 | Multiple Sclerosis |