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. 2022 Oct 27;5(10):e2238880. doi: 10.1001/jamanetworkopen.2022.38880

Table 1. Genome-Wide Significant Maximum Habitual Alcohol Intake Loci in the Cross-Ancestry GWAS, European GWAS, African Ancestry GWAS, and MaxAlc MTAG GWAS.

Chr Position Marker name A1 A2 Nearest gene Direction or MAFa P value SNVs, No. GWAS SNVs, No. IS SNVs, No. Lead SNVs, No.
Cross-ancestry GWAS
4 100239319 rs1229984 C T ADH1B -? 2.46 × 10−101 529 393 22 9
4 103188709 rs13107325 T C SLC39A8 9.40 × 10−15 23 23 4 1
17 44305199 rs570285046 C T CRHR1 ++ 2.12 × 10−14 3590 3538 29 3
7 135162897 rs2551763 T C CNOT4 -? 1.29 × 10−9 29 18 1 1
9 30359634 rs13297433 A G snoU13 ++ 2.01 × 10−9 76 73 2 1
11 47392114 rs7928419 A G SPI1 ++ 2.29 × 10−9 196 172 3 1
1 7830262 rs2153733 C T CAMTA1 +? 1.36 × 10−8 1 1 1 1
19 37504953 rs826323 A G ZNF420 ++ 1.39 × 10−8 162 153 1 1
9 33094361 rs56175925 A G B4GALT1 ?+ 1.82 × 10−8 5 5 1 1
10 10704659 rs34165302 C CA RP1-186E20.1 -? 2.08 × 10−8 87 35 1 1
10 110572259 rs1577857 G T RP11-655H13.2 +? 2.47 × 10−8 100 82 1 1
2 104056769 rs6752675 A G AC092568.1 2.57 × 10−8 196 170 1 1
2 27730940 rs1260326 C T GCKR 2.63 × 10−8 9 9 1 1
11 113392994 rs2514218 T C DRD2 4.59 × 10−8 25 23 1 1
European-ancestry GWAS
4 100239319 rs1229984 C T ADH1B 0.04 3.12 × 10−101 420 275 14 8
4 103188709 rs13107325 T C SLC39A8 0.08 6.78 × 10−15 24 24 2 1
17 43810896 rs77804065 T C CRHR1 0.23 6.04 × 10−14 3839 3533 4 2
11 47676170 rs7107356 G A AGBL2 0.5 1.43 × 10−10 422 313 3 1
7 135162897 rs2551763 T C CNOT4 0.41 1.30 × 10−9 43 19 1 1
1 7830262 rs2153733 C T CAMTA1 0.19 1.36 × 10−8 35 31 1 1
10 10714452 rs145961009 C CTT RP1-186E20.1 0.22 1.73 × 10−8 133 42 1 1
9 30346448 rs4879424 C T snoU13 0.15 2.18 × 10−8 190 169 1 1
10 110572259 rs1577857 G T RP11-655H13.2 0.26 2.47 × 10−8 122 102 1 1
2 27730940 rs1260326 C T GCKR 0.42 4.53 × 10−8 18 18 1 1
African-ancestry GWAS
4 100229017 rs2066702 A G ADH1B 0.19 6.30 × 10−17 109 103 7 1
9 33094361 rs56175925 A G B4GALT1 0.02 1.83 × 10−8 6 5 1 1
MTAG
4 100239319 rs1229984 T C ADH1B 0.04 3.35 × 10−176 1291 646 26 9
4 103188709 rs13107325 T C SLC39A8 0.08 6.01 × 10−36 75 26 6 1
2 27730940 rs1260326 T C GCKR 0.41 2.72 × 10−21 261 98 4 1
4 39423789 rs4975013 A G KLB 0.39 1.44 × 10−19 64 27 4 1
11 113364691 rs17602038 T C DRD2 0.37 2.62 × 10−16 70 36 3 2
11 47406592 rs11039216 T C RP11-750H9.5 0.47 1.07 × 10−15 519 245 5 1
17 44083402 rs1991556 A G MAPT 0.23 2.25 × 10−15 3854 2089 2 1
10 110572259 rs1577857 T G RP11-655H13.2 0.26 6.44 × 10−15 494 304 2 1
2 104361420 rs9308868 A G AC013727.1 0.49 4.88 × 10−13 518 329 3 1
14 58765903 rs61974485 T C ARID4A 0.28 1.02 × 10−12 117 5 1 1
2 45139904 rs472140 T C RP11-89K21.1 0.42 1.11 × 10−11 50 5 2 1
7 135119417 rs2551774 A G CNOT4 0.41 1.50 × 10−11 43 14 1 1
10 10688361 rs7910201 A G RP1-186E20.1 0.25 6.36 × 10−11 168 69 2 1
16 53834607 rs7188250 T C FTO 0.41 8.06 × 10−10 106 82 1 1
7 153487944 rs2098112 A G DPP6 0.47 8.99 × 10−10 112 2 1 1
19 49244219 rs2307018 A C IZUMO1 0.43 9.98 × 10−10 59 21 1 1
1 66503517 rs1354063 T C PDE4B 0.47 1.21 × 10−9 224 81 3 1
15 47681384 rs8033799 A C CTD-2050N2.1 0.21 1.86 × 10−9 157 65 2 1
5 153364650 rs2245405 A G FAM114A2 0.45 2.24 × 10−9 70 32 1 1
22 41789408 rs4822028 A G TEF 0.23 7.97 × 10−9 762 503 2 2
12 81602449 rs1921035 A G ACSS3 0.48 8.44 × 10−9 100 55 1 1
2 144225215 rs13024996 A C RP11-570L15.2 0.36 8.56 × 10−9 29 7 1 1
13 97019647 rs1925104 T G HS6ST3 0.33 1.37 × 10−8 100 56 1 1
8 21831385 rs1484162 A G XPO7 0.41 1.49 × 10−8 56 15 1 1
2 138197269 rs10496771 T C THSD7B 0.25 1.56 × 10−8 222 84 1 1
20 18546199 rs6045466 T C LINC00493 0.47 1.92 × 10−8 150 102 1 1
2 58042241 rs1402398 A G CTD-2026C7.1 0.39 2.00 × 10−8 268 55 2 1
7 117576675 rs6466637 A G AC007568.1 0.28 2.00 × 10−8 39 22 1 1
7 73015369 rs13240065 A G MLXIPL 0.12 2.95 × 10−8 66 46 1 1
2 204123832 rs56059523 T C CYP20A1 0.11 3.17 × 10−8 18 5 1 1
3 18793340 rs9835977 T C AC144521.1 0.30 3.57 × 10−8 79 44 1 1

Abbreviations: +, positive; –, negative; ?, not present; A, allele; Chr, chromosome; GWAS, genome-wide association studies; IS, independently significant; MAF, minor allele frequency; MTAG, multitrait analysis of genome-wide association studies; SNV, single nucleotide variant.

a

For the cross-ancestry GWAS, direction is shown; for European-ancestry GWAS, African-ancestry GWAS, and MTAG, MAF is shown.