Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10501439
TENM4
1.000 0.040 11 79374802 intron variant A/G snv 0.18 1
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10509129
ANK3
1.000 0.040 10 60311283 intron variant G/A;T snv 1
rs10511083
CADM2
1.000 0.040 3 85521809 intron variant A/G snv 0.51 1
rs10512928
ADCY2
1.000 0.040 5 7546298 intron variant C/T snv 0.15 1
rs10513249 1.000 0.040 9 114541631 intergenic variant C/A;G snv 1
rs1051375
CACNA1C ; CACNA1C-AS1
1.000 0.040 12 2679713 synonymous variant G/A snv 0.68 0.57 1
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs1062613
HTR3A
0.807 0.080 11 113975284 5 prime UTR variant T/C snv 0.79 0.71 7
rs1064395
NCAN
0.882 0.120 19 19250926 3 prime UTR variant G/A snv 0.24 3
rs10744560
CACNA1C ; CACNA1C-IT3
0.882 0.040 12 2277933 intron variant C/G;T snv 3
rs10745843
LOC101928937 ; ANKS1B
0.925 0.040 12 99102252 intron variant G/A snv 0.55 2
rs10748045
GRIP1
0.925 0.040 12 66422359 intron variant A/G snv 0.41 3
rs10761473
ANK3
1.000 0.040 10 60300624 intron variant C/G snv 0.12 1
rs10761482
ANK3
0.851 0.120 10 60325579 intron variant T/C snv 0.70 4
rs10774035
CACNA1C
0.925 0.040 12 2259508 intron variant C/A;T snv 2
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs10792421
MARK2
0.925 0.080 11 63837705 upstream gene variant G/A snv 0.47 2
rs10807187
MDGA1
1.000 0.040 6 37661874 intron variant G/A;T snv 0.35 1
rs10821736
ANK3
1.000 0.040 10 60345295 intron variant C/T snv 0.12 1
rs10821745
ANK3
1.000 0.040 10 60376448 intron variant T/G snv 9.7E-02 1
rs10821748
ANK3
1.000 0.040 10 60393180 intron variant G/C snv 0.12 1
rs10821789
ANK3
1.000 0.040 10 60525580 intron variant G/A snv 9.2E-02 1