Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3748960
ERBB4
0.925 0.040 2 211383109 3 prime UTR variant C/T snv 0.96 2
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs4819554
IL17RA
0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs1595065
ERBB4
0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2
rs7311358
SLCO1B3-SLCO1B7 ; SLCO1B3
0.827 0.160 12 20862826 missense variant G/A snv 0.81 0.72 6
rs6026584
GNAS
0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs9909004
PRKCA
0.925 0.040 17 66310015 intron variant C/T snv 0.59 2
rs9303504
PRKCA
0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17