Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs143396368
FXN
0.807 0.200 9 69072623 missense variant G/A;C snv 3.2E-05; 8.0E-06 7
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5
rs778294
DAOA ; DAOA-AS1
0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs6465084
LOC105375382 ; GRM3
0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs61749465
MCPH1
0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5
rs3924999
NRG1
0.851 0.040 8 32595840 missense variant G/A snv 0.40 0.31 5
rs1867283
NTRK2
0.925 0.080 9 84835851 intron variant G/A snv 0.39 5