Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4926499
ZNF692
1 248861710 intron variant G/C snv 0.87 1
rs434578
FNDC1
6 159272188 downstream gene variant C/T snv 0.86 1
rs1764975 20 4120643 upstream gene variant T/A snv 0.85 1
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs2014912
ARHGAP24
4 85794517 intron variant T/C snv 0.84 1
rs912434
LRCH1
13 46615793 intron variant G/T snv 0.84 1
rs2480171
LATS2
13 20985719 intron variant T/C snv 0.84 1
rs1489486
TTN
2 178820256 intron variant A/G snv 0.83 1
rs2469997 8 119341027 intergenic variant G/C snv 0.83 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs476636
ARHGEF12
11 120455568 intron variant G/A snv 0.82 1
rs4335411
PGBD2
1.000 1 248897507 regulatory region variant G/A snv 0.82 3
rs9872857
LINC02052
3 186489773 intron variant A/T snv 0.82 1
rs284844
WBP1L
10 102794772 intron variant A/G snv 0.82 3
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 4
rs7555285
IRF6
1 209797010 intron variant G/C snv 0.81 1
rs1257310 14 99344090 intergenic variant C/A snv 0.81 1
rs1882289
ZBTB20
3 114742361 intron variant G/A snv 0.81 1
rs7158754
EVL
14 100117012 intron variant A/G snv 0.81 1
rs2920899
RTN4
2 55052545 intron variant G/T snv 0.81 1
rs4143175
LOC105369813
12 67388617 regulatory region variant T/C snv 0.80 1
rs11187142 10 92708928 downstream gene variant T/C snv 0.80 1
rs42398
LOC102724748 ; ERAP1
5 96784751 intron variant C/T snv 0.80 1
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs4913007 5 144846912 intergenic variant C/T snv 0.80 1