Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs439558
LINC02210 ; LINC02210-CRHR1
1.000 0.080 17 45640437 non coding transcript exon variant T/C snv 0.16 2
rs448830
LINC02210-CRHR1 ; LINC02210
1.000 0.080 17 45647846 non coding transcript exon variant G/A snv 0.14 2
rs4620530
CHRM3 ; CHRM3-AS1
0.925 0.080 1 239900521 intron variant T/G snv 0.44 2
rs4679904 0.925 0.080 3 160623108 intergenic variant C/G;T snv 2
rs485499
LINC01100 ; IL12A-AS1
0.925 0.080 3 160028076 intron variant T/C snv 0.29 2
rs4938534
BTG4 ; POU2AF1
0.925 0.080 11 111404408 intron variant G/A snv 0.56 2
rs4979467
DELEC1
0.925 0.080 9 114867763 intron variant C/T snv 0.52 2
rs538147
RPS6KA4
0.925 0.080 11 64362250 intron variant G/A snv 0.29 2
rs5757611 1.000 0.080 22 39312352 downstream gene variant C/T snv 0.19 2
rs6441286
IL12A-AS1
0.925 0.080 3 160011091 intron variant T/G snv 0.36 2
rs6478106 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 2
rs6503513
MED1
1.000 0.080 17 39405360 3 prime UTR variant A/G snv 0.33 2
rs6890853
LOC105374724
0.925 0.080 5 35852209 upstream gene variant G/A snv 0.25 2
rs70602
LRRC37A2 ; WNT3
1.000 0.080 17 46782349 intron variant T/C snv 0.84 2
rs7503377
CDK12
1.000 0.080 17 39552588 intron variant T/C;G snv 2
rs7665590
EIF4E
0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56 2
rs767058
LOC105371800 ; MAPT
1.000 0.080 17 45921401 intron variant T/C snv 0.14 2
rs7687
MAPT
1.000 0.080 17 46025930 3 prime UTR variant T/C snv 0.14 2
rs7863183
DELEC1
0.925 0.080 9 114880138 intron variant T/A;C snv 2
rs8017161
EXOC3L4
0.925 0.080 14 103096858 intron variant G/A snv 0.38 2
rs8069074
CDK12
1.000 0.080 17 39529148 intron variant A/G snv 0.79 2
rs8070942
KANSL1
1.000 0.080 17 46131308 intron variant G/T snv 0.23 2
rs8073907
FBXL20
1.000 0.080 17 39267896 intron variant C/T snv 0.78 2
rs860413 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 2
rs916793
MAPT-AS1
1.000 0.080 17 45877320 intron variant G/A snv 0.14 2