Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs7212450
LOC105371490
1.000 0.040 17 2688646 intron variant G/A;C snv 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs7939345 1.000 0.040 11 47959016 intergenic variant T/A;G snv 3
rs8100891 1.000 0.040 19 32338607 intergenic variant C/A;G snv 3
rs10156548 1.000 0.040 9 23318435 intron variant G/C;T snv 2
rs1055447
ARFGAP2 ; C11orf49
1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 2
rs11599236
SORCS3
1.000 0.040 10 104694914 intron variant T/C;G snv 2
rs11605020
LOC105369562
1.000 0.040 11 127110970 intron variant G/A;C snv 2
rs11693031
ERBB4
1.000 0.040 2 211813206 intron variant A/G;T snv 2
rs11826064 1.000 0.040 11 50818695 intergenic variant C/A;T snv 2
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs12938775
PAFAH1B1
1.000 0.040 17 2671527 intron variant G/A;T snv 2
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv 2
rs1360380 1.000 0.040 9 23378490 intron variant G/A;T snv 2
rs1422192
LINC00461
1.000 0.040 5 88663205 intron variant G/A;T snv 2
rs1427027 1.000 0.040 18 37666359 intron variant C/G;T snv 2
rs1490176
SORCS3
1.000 0.040 10 104800467 intron variant T/A;G snv 2
rs17487484
DCC
1.000 0.040 18 53196913 intron variant T/A;G snv 2
rs1782179 1.000 0.040 14 41224737 intergenic variant T/A;C snv 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs1875560
DCC
1.000 0.040 18 53434318 intron variant A/C;G snv 2
rs1885884
HTR2A ; HTR2A-AS1
13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs200312707
CDH8
1.000 0.040 16 62031776 intron variant TA/- del 2
rs2278609
PLCL2 ; LOC105376972
1.000 0.040 3 16882947 intron variant C/A;G;T snv 2