Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs200312707
CDH8
1.000 0.040 16 62031776 intron variant TA/- del 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs1800866
SIGMAR1
0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 8
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 5
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs76371172
OTUD7A ; LOC105370753
0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs806371
CNR1
0.882 0.040 6 88146644 intron variant T/G snv 0.18 4
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs75782365
BTN3A1
0.925 0.040 6 26408323 intron variant T/G snv 5.2E-02 3
rs11214607
DRD2
1.000 0.040 11 113441417 intron variant T/G snv 0.16 2
rs13413953
ARHGAP15
1.000 0.040 2 143479467 intron variant T/G snv 0.25 2
rs1364043 0.925 0.040 5 63955024 downstream gene variant T/G snv 0.24 2
rs149702363
LOC101929006
0.925 0.120 6 29257248 intron variant T/G snv 3.8E-02 2
rs150814685 0.925 0.120 6 28728995 upstream gene variant T/G snv 3.4E-02 2
rs1542212
ARPP21
1.000 0.040 3 35642443 intron variant T/G snv 0.36 2
rs17508548
GABBR1
1.000 0.040 6 29595290 intron variant T/G snv 0.12 2
rs190544851 1.000 0.040 21 38360474 intergenic variant T/G snv 4.8E-03 2
rs2149351 1.000 0.040 9 117739366 intron variant T/G snv 0.81 2