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. 2020 May 1;11:2175. doi: 10.1038/s41467-020-15932-3

Table 1.

Top association SNPs for independent loci for WMH meta-analysis.

CHR:BP rsID A1/A2 A1_FREQ WMH_P FA_P MD_P HGNC genes Novel
1:197499003 rs12120143 T/C 0.03 6.45 × 10−09 3.78 × 10−02 3.79 × 10−01 DENND1B Yes
2:43118872 rs7566761 A/G 0.20 7.62 × 10−13 1.95 × 10−01 6.57 × 10−01 AC098824.6a No
2:56128091 rs7596872 A/C 0.10 2.06 × 10−20 3.92 × 10−01 1.48 × 10−02 EFEMP1 No
2:188003118 rs17576323 C/T 0.20 3.15 × 10−08 3.38 × 10−01 6.92 × 10−01 AC007319.1 Yes
2:203916487 rs72934505 G/T 0.13 4.31 × 10−13 7.34 × 10−08 7.28 × 10−05 ICA1L, WDR12, CARF, NBEAL1, CYP20A1 No
3:183380035 rs830179 A/G 0.32 4.67 × 10−09 3.21 × 10−01 1.11 × 10−03 KLHL24 Yes
5:121510586 rs17148926 C/A 0.17 4.07 × 10−09 1.54 × 10−03 4.46 × 10−05 CTC-441N14.4 Yes
6:151016058 rs275350 C/G 0.41 8.83 × 10−17 3.96 × 10−03 4.54 × 10−05 PLEKHG1 No
7:100361391 rs3215395 ID/G 0.29 2.18 × 10−08 1.21 × 10−02 4.42 × 10−03 ZAN Yes
10:105459116 rs4630220 A/G 0.29 1.21 × 10−14 2.88 × 10−03 3.32 × 10−05 SH3PXD2A No
13:111040681 rs11838776 A/G 0.28 7.90 × 10−11 1.97 × 10−01 1.03 × 10−02 COL4A2 No
14:100581636 rs11160570 T/C 0.26 6.10 × 10−13 1.09 × 10−02 3.19 × 10−05 EVL, DEGS2 No
15:65326833 rs12906662 A/T 0.47 6.42 × 10−09 8.81 × 10−01 1.85 × 10−01 MTFMT, SLC51B Yes
16:51451683 rs17616633 T/C 0.44 7.33 × 10−11 2.01 × 10−01 4.97 × 10−02 RP11-437L7.1a Yes
16:87237568 rs12928520 T/C 0.44 1.26 × 10−13 8.18 × 10−01 2.10 × 10−01 C16orf95 Yes
17:19224397 rs6587216 G/C 0.19 8.01 × 10−09 1.72 × 10−01 1.57 × 10−02 EPN2 Yes
17:43128906 rs8071429 T/A 0.37 2.61 × 10−16 9.17 × 10−05 4.14 × 10−06 DCAKD, NMT1 No
17:73882148 rs7214628 G/A 0.19 4.99 × 10−36 1.06 × 10−01 1.75 × 10−03 WBP2, TRIM47, TRIM65 No
19:45411941 rs429358 C/T 0.15 1.15 × 10−09 1.87 × 10−02 6.92 × 10−04 APOE Yes

CHR:BP chromosome and position in bp, rsID the SNP ID, A1/A2, tested and non-tested alleles (ID is for insertion/deletions), A1_FREQ the allele frequency of the tested allele in the UK Biobank population for WMH, WMH_P, FA_P and MD_P the p-values for WMH, FA and MD respectively, HGNC genes the nearest genes to the lead SNP and its proxies (r2≥ 0.8), genes symbols are in italic to comply with the nomenclature, Novel this column indicated if the association has already been described in previous GWAS.

aThe lead SNP and/or proxies lie in an intergenic region.