Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10400694 1.000 0.080 14 84147550 intergenic variant G/C;T snv 1
rs11052413 1.000 0.080 12 33053704 intergenic variant T/G snv 0.58 1
rs11214109 1.000 0.080 11 112173503 intron variant C/G;T snv 1
rs11498973 1.000 0.080 10 84732025 intergenic variant A/C snv 0.19 1
rs116902978 1.000 0.080 13 65253855 regulatory region variant T/G snv 2.5E-02 1
rs13040307 1.000 0.080 20 46114008 upstream gene variant C/T snv 0.19 1
rs1491034 1.000 0.080 13 90049366 intergenic variant A/G snv 0.17 1
rs1570063 1.000 0.080 6 49669314 intergenic variant T/A;C snv 1
rs2634074 1.000 0.080 4 110755885 intergenic variant T/A snv 0.66 1
rs2825226 1.000 0.080 21 18909856 intergenic variant G/A snv 0.27 1
rs34354898 1.000 0.080 6 87129144 intergenic variant G/A;T snv 1
rs360139 1.000 0.080 11 9753544 upstream gene variant A/G snv 0.62 1
rs59920395 1.000 0.080 5 3650229 intergenic variant C/T snv 6.0E-02 1
rs61937565 1.000 0.080 12 38997354 upstream gene variant T/C snv 0.11 1
rs61937587 1.000 0.080 12 39004369 intergenic variant G/A snv 0.15 1
rs7007329 1.000 0.080 8 42212037 upstream gene variant C/A;G;T snv 1
rs73712231 1.000 0.080 8 137203404 intergenic variant C/T snv 9.9E-02 1
rs9301654 1.000 0.080 13 90142152 intergenic variant A/G snv 0.20 1
rs9533290 1.000 0.080 13 30863403 intergenic variant A/G snv 0.64 1
rs74475935
ABCC1
1.000 0.080 16 15961249 intron variant C/G snv 4.5E-03 1
rs4341
ACE
1.000 0.080 17 63488629 3 prime UTR variant G/C snv 0.50 1
rs980857256
ACE
1.000 0.080 17 63485015 stop gained C/T snv 8.2E-06 6.3E-05 1
rs35724886
ACOT4
1.000 0.080 14 73593804 missense variant C/A snv 4.9E-02 0.15 1
rs12438353
AGBL1
1.000 0.080 15 86771849 intron variant C/T snv 0.38 1
rs10744777
ALDH2
1.000 0.080 12 111795214 intron variant T/C snv 0.53 1