Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs721970 1.000 0.040 20 33315727 upstream gene variant A/G snv 0.96 1
rs1885120
LOC107985393 ; MIR499A ; MYH7B
1.000 0.040 20 34989186 intron variant C/G snv 0.96 2
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs6058339
PHF20
1.000 0.040 20 35872557 intron variant C/T snv 0.94 1
rs4911442
NCOA6
1.000 0.040 20 34767243 intron variant G/A snv 0.93 2
rs291671
CDK5RAP1
1.000 0.040 20 33363039 intron variant G/A snv 0.92 2
rs2995264
STN1
0.851 0.080 10 103909085 intron variant G/A snv 0.88 4
rs6431588
ILKAP
0.925 0.040 2 238185147 intron variant T/C;G snv 0.86 0.85 2
rs910871
NCOA6
1.000 0.040 20 34745404 intron variant C/A snv 0.85 1
rs35390
SLC45A2
1.000 0.040 5 33955221 intron variant C/A snv 0.81 1
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs8059973
DBNDD1
1.000 0.040 16 90013126 intron variant A/G snv 0.78 1
rs2306574
PRKCD
1.000 0.040 3 53188745 synonymous variant C/T snv 0.75 0.75 1
rs4911414 0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73 5
rs222016
GC
0.882 0.120 4 71769258 intron variant G/A snv 0.72 3
rs700635
FLACC1
0.925 0.040 2 201288502 3 prime UTR variant C/A snv 0.72 3
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1015363 1.000 0.040 20 34150529 intergenic variant G/A snv 0.69 1
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs498136 0.851 0.080 11 69552350 intergenic variant A/C snv 0.68 4
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs869330
MTAP
0.925 0.080 9 21804618 intron variant A/G snv 0.62 2
rs12380505
KHSRPP1
1.000 0.040 9 21695894 non coding transcript exon variant A/G snv 0.62 1