Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4954218
MAP3K19
0.925 0.080 2 135045855 intron variant G/T snv 0.83 5
rs12147254
TRAF3
0.851 0.240 14 102799329 intron variant G/A snv 0.23 4
rs1481017
ABCG2
0.882 0.160 4 88176325 intron variant C/T snv 0.59 4
rs1498373
DDAH1
0.882 0.120 1 85324950 intron variant G/A snv 0.28 4
rs2622590
XKR4
0.925 0.080 8 55445714 intron variant G/A snv 0.15 4
rs2622629
ABCG2
0.882 0.160 4 88172912 intron variant T/C snv 0.28 4
rs4971059
TRIM46
0.851 0.200 1 155176305 intron variant G/A snv 0.34 4
rs652722
PAX6-AS1 ; PAUPAR
1.000 0.040 11 31883988 intron variant C/T snv 0.32 4
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs10054105
STARD4-AS1
0.925 0.080 5 111573636 intron variant T/G snv 0.17 3
rs10821871
A1CF
0.882 0.160 10 50824350 intron variant T/C snv 0.22 3
rs10994720
A1CF
0.882 0.160 10 50852341 intron variant G/A snv 0.21 3
rs11709077
PPARG
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs11815391
A1CF
0.882 0.160 10 50818978 intron variant A/G snv 0.26 3
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs12199222
NUP153
1.000 0.040 6 17699091 intron variant G/A;T snv 3
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs1481014
ABCG2
0.882 0.160 4 88175999 intron variant C/A;T snv 0.24 3
rs17036188
PPARG
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs17036328
PPARG
1.000 0.040 3 12348985 intron variant T/C snv 0.14 3
rs17056278
EBF1
0.925 0.040 5 158825430 intron variant C/G snv 5.3E-02 3
rs17806888
SUCLG2
1.000 0.040 3 67365898 intron variant T/C snv 9.1E-02 3
rs2127863
ABCG2
0.882 0.160 4 88190316 intron variant T/C snv 0.84 3
rs324148
SLC29A1
0.882 0.280 6 44228841 intron variant T/C snv 0.78 3
rs41520844
WRN
0.882 0.080 8 31135670 intron variant A/T snv 7.1E-02 3