Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs352165
ALAS1
0.925 0.120 3 52208886 intron variant A/C;G snv 0.47 2
rs420259
PALB2
0.925 0.040 16 23622705 intron variant A/C;G snv 2
rs11013860
CACNB2
1.000 0.040 10 18365098 intron variant A/C;G snv 0.11 1
rs2070615
CACNB3
1.000 0.040 12 48824388 intron variant A/C;G snv 4.7E-06; 0.58 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs329319
JADE2
1.000 0.040 5 134570919 intron variant A/C;G;T snv 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs300774 0.925 0.040 2 112496 intergenic variant A/C;T snv 3
rs12487445
PBRM1
0.925 0.040 3 52584303 intron variant A/C;T snv 2
rs11237799
TENM4
1.000 0.040 11 79356427 intron variant A/C;T snv 1
rs4447398
STARD9
1.000 0.040 15 42612706 intron variant A/C;T snv 1
rs6079468
MACROD2
1.000 0.040 20 14517750 intron variant A/C;T snv 1
rs6804845
CADM2
1.000 0.040 3 85514696 intron variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9