Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
rs2793094
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231741236 intron variant G/A snv 0.97 3
rs33990840
AVPR1B
0.925 0.080 1 206116320 missense variant C/G;T snv 5.0E-02; 2.8E-05 3
rs4658966
DISC1 ; TSNAX-DISC1 ; DISC1-IT1
0.925 0.080 1 231942868 intron variant T/C snv 0.19 3
rs6704393
NOS1AP
0.925 0.080 1 162182266 intron variant C/A;T snv 3
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1013940
SLC5A7
0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs2300478
MEIS1
0.851 0.120 2 66554321 intron variant T/G snv 0.21 6
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs4672619
ERBB4
0.882 0.160 2 211592470 intron variant C/A;G snv 4
rs1364647619
POMC
0.925 0.080 2 25161334 missense variant C/T snv 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs12630592
GSK3B
0.851 0.080 3 120049399 intron variant G/A;T snv 5