Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 8
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 8
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 7
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 7
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs1178979
BAZ1B
0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs11974409
TBL2
0.925 0.120 7 73575060 intron variant A/G snv 0.16 6
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 6
rs13232120
TBL2
0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11 6
rs17145713
BAZ1B
0.925 0.120 7 73490480 intron variant C/T snv 0.21 6
rs1919127
C2orf16
0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 6
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6
rs2911711 0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58 6