Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs6857715
NPY2R ; LOC107986321
0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 5
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs12649507
CLOCK
0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs2273816
KPNA3
0.851 0.080 13 49719920 intron variant G/A;C snv 4
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs11155372
UTRN
0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs352759
TUSC3
0.925 0.040 8 15742205 intron variant T/A snv 3
rs6063349
CSE1L
0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs6883197
CMYA5
0.882 0.040 5 79695550 intron variant A/C;G snv 3
rs7189979
SNX29
0.925 0.040 16 12536330 intron variant A/C;G;T snv 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs760161369
MTHFR
0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 3
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3