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letter
. 2006 Oct;55(10):1527–1528. doi: 10.1136/gut.2006.100297

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.

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