Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 3
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29 3
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs1884429 1 11052779 downstream gene variant T/C snv 0.74 2
rs212526
ECE1
1 21258448 intron variant T/C snv 0.68 2
rs2885697
SCMH1
1.000 0.080 1 41078607 intron variant G/T snv 0.72 2
rs3765350
WNT4
1 22120823 intron variant A/G snv 0.22 2
rs55745410
PHC2
1 33337216 intron variant A/G snv 0.28 2
rs10917220 1 22356912 intergenic variant T/C snv 0.65 1
rs1108548
LINC02869
1 218461445 intron variant A/G snv 0.40 1
rs111352324
FAF1
1 50755008 intron variant T/C snv 8.7E-02 1
rs113422653
LOC105373258 ; LINC02774
1 243978778 intron variant G/A snv 3.8E-02 1
rs12040325
NADK
1 1770997 intron variant G/A snv 0.39 1
rs12409277 1 3041036 intergenic variant T/C snv 0.17 1
rs2474944 1 118342903 intergenic variant T/A;C;G snv 1
rs2644111
IPO9
1 201832924 intron variant G/A snv 0.28 1
rs28521412
LOC105371438 ; ANXA9
1 150982244 upstream gene variant G/A snv 8.0E-03 1
rs60401266
LNCTAM34A ; MIR34AHG
1 9192362 intron variant G/A;T snv 1
rs61775431 1 26084784 intergenic variant T/G snv 0.15 1
rs61838774
LYPLAL1 ; LYPLAL1-AS1
1 219440433 intron variant A/G snv 0.27 1
rs76798800
DCST2
1 155022502 intron variant G/A;T snv 1
rs778416 1 56178475 intron variant A/G snv 0.38 1