Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766288
TSNAX-DISC1 ; TSNAX
0.790 0.080 1 231557942 intron variant G/T snv 0.40 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs2076137
MLC1
0.807 0.080 22 50077337 intron variant C/T snv 0.14 6
rs2235349
MLC1
0.807 0.080 22 50079810 intron variant T/C snv 0.22 6
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs2802292
FOXO3
0.851 0.160 6 108587315 intron variant G/T snv 0.50 6
rs2812393
TSNAX-DISC1 ; DISC1
0.807 0.080 1 231777927 intron variant G/C snv 0.61 6
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs4500567
TSPAN8
0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs4774388
RORA
0.807 0.200 15 61174799 intron variant C/T snv 0.81 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs707284
ERBB4
0.807 0.080 2 211974321 intron variant T/A;C snv 6
rs951266
CHRNA5
0.882 0.080 15 78586199 intron variant G/A snv 0.26 6
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
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5