Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs10462023
PER2
2 238275940 intron variant G/A snv 0.31 0.27 1
rs1655285
TSNAX-DISC1 ; TSNAX
1 231563728 intron variant G/C snv 9.5E-02 1
rs2789588 6 72433995 intergenic variant A/C snv 0.26 1
rs4583255
TAOK2
16 29977620 intron variant A/G snv 0.36 1
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs3924999
NRG1
0.851 0.040 8 32595840 missense variant G/A snv 0.40 0.31 5
rs6465084
LOC105375382 ; GRM3
0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 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
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5