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. Author manuscript; available in PMC: 2018 Apr 30.
Published in final edited form as: Nat Genet. 2017 Oct 30;49(12):1722–1730. doi: 10.1038/ng.3978

Table 4.

Loci where East Asian and GLGC samples identified the same putatively functional protein-altering variant

Gene rsID Position Variant Alleles Trait Study BETA S.E. P AAF Variance Explained Note*
GCKR rs1260326 2:27730940 p.Leu446Pro C/T TG GLGC −0.121 0.003 0.00 0.628 0.64% Protein-altering is top
TG Asian −0.114 0.007 1.26×10−62 0.496 0.64% Protein-altering is top
MLXIPL rs35332062 7:73012042 p.Ala358Val A/G TG GLGC −0.124 0.004 5.22×10−205 0.117 0.30% Protein-altering is top
TG Asian −0.109 0.011 2.03×10−23 0.109 0.23% Explaining index
LPL rs328 8:19819724 p.Ser474* G/C TG GLGC −0.184 0.004 0.00 0.098 0.58% Explaining index
TG Asian −0.169 0.012 1.93×10−45 0.095 0.46% Explaining index
GPAM rs2792751 10:113940329 p.Ile43Val C/T TC GLGC −0.028 0.003 7.14×10−22 0.728 0.03% Explaining index
TC Asian −0.043 0.007 5.67×10−9 0.706 0.07% Protein-altering is top
HNF1A rs1169288 12:121416650 p.Ile27Leu C/A TC GLGC 0.037 0.003 9.99×10−40 0.333 0.06% Protein-altering is top
TC Asian 0.038 0.007 4.86×10−8 0.404 0.07% Protein-altering is top
TM6SF2 rs58542926 19:19379549 p.Glu167Lys T/C TC GLGC −0.129 0.005 7.03×10−155 0.074 0.22% Protein-altering is top
TC Asian −0.066 0.013 4.25×10−7 0.070 0.06% Protein-altering is top
APOE rs7412 19:45412079 p.Arg176Cys T/C LDL-C GLGC −0.539 0.006 0.00 0.075 3.80% Independent of index
LDL-C Asian −0.472 0.016 4.87×10−197 0.088 3.49% Protein-altering is top

AAF, alternative allele frequency.

Position is reported in human genome build hg19.

Alleles are listed as alternative / reference allele on the forward strand of the reference genome.

*

Protein-altering is top: protein-altering variants are the most significant variants in the known loci.

Explaining index: Conditional on the coding variants, the adjusted P for index variants >0.01.

Independent of index: Conditional on the index variants, the adjusted P for coding variants with exome-wide significance.