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.