Table 1 Allele frequencies of TNFSF15.
SNP | dbSNP | Location | Allele1 | Allele2 | Frequency of allele2 (%)/OR/p value | ||
---|---|---|---|---|---|---|---|
HCs (n = 277) | CD (n = 286) | UC (n = 263) | |||||
tnfsf15_36 | rs7848647 | 5′‐flanking region | G | A | 39.0 | 25.7 (OR = 1.85, p = 1.84×10−6) | 36.3 (NS) |
tnfsf15_35 | rs6478109 | 5′‐flanking region | C | T | 39.0 | 25.7 (OR = 1.85, p = 1.84×10−6) | 36.3 (NS) |
tnfsf15_33 | rs6478108 | Intron 1 | A | G | 51.8 | 37.6 (OR = 1.78, p = 1.60×10−6) | 52.3 (NS) |
tnfsf15_31 | rs4979462 | Intron 1 | A | G | 39.5 | 26.2 (OR = 1.84, p = 1.98×10−6) | 36.5 (NS) |
tnfsf15_28 | – | Intron 3 | C | T | 53.1 | 38.8 (OR = 1.78, p = 1.58×10−6) | 52.3 (NS) |
tnfsf15_26 | rs3810936 | Exon 4 (Val201Val) | G | A | 40.3 | 26.9 (OR = 1.83, p = 2.15×10−6) | 36.3 (NS) |
SNP, single nucleotide polymorphism; HCs, healthy controls; CD, Crohn's disease; UC, ulcerative colitis; NS, no significant. OR, odds ratio.