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. 2018 Dec 27;8:18088. doi: 10.1038/s41598-018-36429-6

Table 2.

Genomic risk loci from the discovery sample which are not genome-wide significant in IGAP.

CHR BP SNP A1/A2 MAF Gene Discovery Replication Combined Dir.
OR p-value OR p-value OR p-value
4 11676144 rs6448807 T/C 0.30 RP11-281P23.2
(HS3ST1)
1.08 2.23E-08 1.03 1.72E-01 1.07 2.48E-08 +++
10 11720308 rs7920721 G/A 0.27 RP11-138I18.2
(USP6NL/ECHDC3)
1.07 1.82E-08 1.06 7.23E-03 1.07 4.84E-10 +++
14 107156009 rs79452530 T/C 0.16 IGHV1-68
(IGHV1-68)
0.89 2.36E-08 0.97 3.08E-01 0.91 1.27E-07
17 56404349 rs2526378 G/A 0.47 BZRAP1-AS1
(BZRAP1)
0.93 3.64E-09 0.99 6.69E-01 0.94 5.30E-08

CHR: chromosome; BP: base pair location; A1/A2: major/minor alleles; MAF: minor allele frequency in 1000 G. Gene: nearest gene and nearest protein-coding gene (in parentheses). OR: odds ratio; Dir.: direction of effects in the two discovery samples (Demgene, IGAP) and the replication sample (Iceland).