Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs10462023
PER2
2 238275940 intron variant G/A snv 0.31 0.27 1
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs1126442
GRIN1 ; LOC105376328
1.000 0.040 9 137156924 missense variant G/A snv 0.26 0.24 2
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs12155594
NRG1
1.000 0.040 8 31749079 intron variant C/T snv 7.8E-02 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614