Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6740706
LRRFIP1
2 237719866 intron variant C/T snv 0.86 1
rs9664222 10 87578876 intergenic variant A/C snv 0.84 1
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs5766691
TBC1D22A
22 47136753 intron variant A/G snv 0.73 1
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs1487614 4 42267463 non coding transcript exon variant T/C snv 0.65 1
rs10256972
C7orf50
7 999367 intron variant A/C snv 0.62 1
rs7874142
COL5A1
9 134812936 intron variant G/A snv 0.62 1
rs2024714
CDH4
20 61637438 intron variant C/T snv 0.60 1
rs432203
TGFA
2 70537556 intron variant C/A snv 0.58 1
rs4148546
ABCC4
13 95028031 intron variant G/A snv 0.55 1
rs13118159
UVSSA
4 1371339 intron variant T/C snv 0.55 1
rs9517320
STK24
13 98474049 intron variant A/C snv 0.55 1
rs2031577 10 4007811 intergenic variant A/G snv 0.53 1
rs4732038
AKR1B15
7 134565570 intron variant A/C snv 0.51 0.52 1
rs4468878
CDH4
20 61353181 intron variant T/C snv 0.51 1
rs6568433
CRYBG1
6 106381662 intron variant T/C snv 0.48 1
rs2826891
NCAM2
21 21537795 intron variant C/T snv 0.43 0.47 1
rs739401
CARS1
11 3015094 intron variant C/T snv 0.45 2
rs12143832 1 21378943 regulatory region variant T/C snv 0.44 1
rs3106598 13 61104778 intron variant G/A snv 0.43 1
rs7315621 12 131600651 upstream gene variant G/A snv 0.41 1
rs4745062
TRPM3
9 71169348 intron variant C/T snv 0.40 1
rs7493138 14 28552722 intergenic variant C/T snv 0.38 1
rs7168365
LOC105370826 ; WDR72
15 53513628 downstream gene variant C/A snv 0.37 1