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. Author manuscript; available in PMC: 2022 Jun 1.
Published in final edited form as: J Invest Dermatol. 2020 Dec 30;141(6):1493–1502. doi: 10.1016/j.jid.2020.11.025

Table 1:

Trans-disease meta-analysis results for loci meeting criteria

Marker ID Chr Position (hg19) Alleles (risk/non-risk) Meta-analysis P-values Meta-analysis Odds Ratios Minor Allele Frequenciesa Nearby Gene BMI Locus?b Newc GWAS Locus?b
P(Psoriasis) P(T2D) P(Both) OR(Psoriasis) OR(T2D) OR(Both) Psoriasis T2D
rs840967 2 65701757 C/A 6.6x10−5 4.4x10−8 9.6x10−9 1.08 1.04 1.06 0.40 0.41 SPRED2 No Psoriasis
rs12265333 10 102011211 A/G 1.6x10−6 7.1x10−7 1.0x10−9 1.12 1.04 1.08 0.49 0.49 CHUK No No
rs685870 11 64111928 T/C 8.5x10−9 7.8x10−5 1.0x10−11 1.13 1.03 1.08 0.31 0.30 PRDX5 Yesd T2D
rs2292749 17 40818584 T/C 4.3x10−6 1.5x10−6 1.5x10−9 1.10 1.04 1.07 0.29 0.30 STAT3 No No

Abbreviations are as follows: Chr, chromosome; OR, odds ratio; p, p-value; T2D, type 2 diabetes; BMI, body mass index; GWS, genome-wide significant (i.e. p<5x10−8).

a

Minor alleles are provided for each entire meta-analysis (cases and controls), rather than specigically for each disease.

b

We determine whether a locus is previously known to be associated with BMI, psoriasis, or T2D according to data from the GIANT and DIAGRAM consortium, as well as a search of the available literature.

c

To our knowledge, previously unreported.

d

The lead marker of the chromosome 11 locus (rs685870) is significantly associated with BMI in the GIANT consortium meta-analysis (2.3x10−9), but its effect (OR=1.01) is in the opposite direction to the signal we identified in our trans-disease meta-analysis (i.e. the risk allele is C rather than T), suggesting it is not in the same haplotype.