Table 1 Information of the single nucleotide polymorphisms (SNPs) in SLC39A8
From: SLC39A8 is a risk factor for schizophrenia in Uygur Chinese: a case-control study
SNP ID | Chromosome | Function | Polymorphism | Call ratea |
|---|---|---|---|---|
rs233814 | 102,287,546 | Intron variant | C/T | 0.996 |
rs233820 | 102,301,031 | Intron variant, UTR variant 3 prime | C/G/A | 0.994 |
rs10014145 | 102,279,420 | Intron variant | A/G | 0.97 |
rs4698844 | 102,296,823 | Intron variant | C/T | 0.995 |
rs151394 | 102,263,495 | Intron variant | C/G | 0.987 |
rs985989 | 102,304,098 | Intron variant | G/T | 0.984 |
rs13114343 | 102,268,259 | Intron variant | A/G | 0.99 |