Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10118776
LOC107987046 ; IL33
1.000 0.080 9 6227418 intron variant G/A snv 0.94 1
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs7519667
WDR64
1.000 0.080 1 241722005 intron variant C/T snv 0.78 1
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs3134425
CRTAM
1.000 0.080 11 122838470 intron variant T/C snv 0.67 1
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs6790167
TP63
0.827 0.080 3 189869485 intron variant A/G snv 0.53 5
rs716274 1.000 0.080 11 103547430 intergenic variant A/G snv 0.51 1
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs402710
CLPTM1L
0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs8049634
LOC654780 ; ADAD2
1.000 0.080 16 84192073 intron variant A/G snv 0.35 1
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs312599 1.000 0.080 5 143998425 intergenic variant C/T snv 0.33 1
rs6104
SERPINB10 ; SERPINB2
0.807 0.160 18 63903295 missense variant C/G snv 0.29 0.28 6
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1778335
PIP4K2A
1.000 0.080 10 22643219 intron variant T/C snv 0.27 1
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 5
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6