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. 2024 Nov 13;15:9839. doi: 10.1038/s41467-024-53595-6

Table 3.

Discovery GWAS, replication and combined meta-analysis results for LOMG

Nearest gene Index SNP CHR BP (GRCh37) A1/A2 FRQ case FRQ control Proxy P OR SE P-rep OR-rep SE-rep P-comb OR-comb SE-comb
PTPN22 rs2476601a 1 114377568 A/G 0.141 0.132 same 9.26e−15 1.47669 0.0503 3.92e−14 1.311637 0.035159 5.11e−27 1.3637 0.0288
CTLA4 rs231779a,b 2 204734487 C/T 0.572 0.515 rs231770 2.66e−06 0.85172 0.0342 2.37e−05 0.910374 0.024511 4.99e−09 0.89003 0.0199
MHC rs72848204a 6 32594073 G/T 0.749 0.697 same 1.20e−23 1.50953 0.0411 2.37e−02 1.049218 0.024296 1.04e−11 1.15281 0.0209
TNFRSF11A rs7239261a 18 60005046 A/C 0.492 0.368 same 1.56e−14 1.29576 0.0337 4.43e−04 1.079214 0.022905 1.50e−12 1.14339 0.0189

The table presents the results from the discovery-, replication-, and combined inverse-variance-weighted fixed-effects meta-analyses.

BP (GRCh37) Base Pair position on Genome Reference Consortium Human Build 37, CHR chromosome, comb combined meta-analysis of discovery and control GWAS results, FRQ frequency.

aPreviously published as genome-wide significant locus.

bWould not withstand a multiple testing correction for 13 million tests (P < 3.85e−9), accounting for the leave-one-out GWAS.