Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199476133
ND3 ; COX3 ; ND4L ; ND4 ; ATP8 ; ATP6
0.742 0.320 MT 8993 missense variant T/C;G snv 18
rs7958904
HOTAIR
0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs1057519736
IDH2
0.752 0.160 15 90088605 missense variant C/G snv 13
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs1052667
ARHGAP35
0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs1056629
MPHOSPH6
0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 6
rs1872328
ACYP2
0.827 0.120 2 54168122 intron variant G/A snv 7.3E-02 6
rs3821204
IL18R1 ; IL1RL1
0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21 6
rs9895829
TP53
0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs1005464
BMP2
0.882 0.040 20 6775501 intron variant G/A snv 0.19 5
rs1060501205
TP53
0.827 0.120 17 7673749 missense variant TG/GT mnv 5
rs1800541
EDN1
0.851 0.120 6 12288986 upstream gene variant T/G snv 0.24 5
rs3178250
BMP2
0.827 0.080 20 6779554 3 prime UTR variant T/C snv 0.21 5
rs4150441
ERCC3
0.882 0.040 2 127283339 intron variant T/C snv 0.37 5
rs6973569
NPSR1-AS1
0.851 0.080 7 34583412 intron variant G/A snv 4.7E-02 5
rs8103851
PRKCG
0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs121913282
PIK3CA
0.882 0.040 3 179221072 missense variant A/C snv 4
rs1253660442
SLC19A1
0.851 0.160 21 45531871 missense variant G/A;C snv 4
rs12602273
TP53
0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs1690916
MDM2
0.882 0.040 12 68841626 3 prime UTR variant G/A snv 0.35 4