Table 1. Dysbindin SNP genotyping in schizophrenia and controls.
valid n | ||||||||
---|---|---|---|---|---|---|---|---|
SNP identification number | SNP | minor allele frequency | SNP location | Chromosome 6 position* | TaqMan SNP assay | custom asay designed to* | 1/1 | 1/2 and 2/2 |
rs2619537 | A/G | 0.12 | 5′ flanking region | 15664413 | AHWR12B (custom) | chr6:15662718-15663518 | 51 | 20 |
rs2743864 | C/T | 0.09 | Intron 3 | 15640281 | C_114533_10 | n/a | 60 | 11 |
rs1047631 | T/C | 0.15 | exon 10 (3′ UTR) | 15523101 | C_7460562_10 | n/a | 52 | 20 |
from the UCSC Genome Browser on Human Feb. 2009 (GRCh37/hg19) Assembly