Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs1001703993
PPOX
0.882 0.120 1 161170696 missense variant G/A;T snv 8.0E-06 1.4E-05 3
rs10086568 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 2
rs1008898
C1GALT1
1.000 0.120 7 7233928 intron variant G/A;T snv 1
rs1047763
C1GALT1
0.925 0.120 7 7243938 3 prime UTR variant G/A snv 0.22 2
rs10488764
FDX1
1.000 0.120 11 110460907 intron variant G/A snv 0.18 1
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs1055901
SERPINB7
1.000 0.120 18 63805221 3 prime UTR variant T/C snv 0.61 1
rs1055902
SERPINB7
1.000 0.120 18 63805309 3 prime UTR variant C/T snv 0.59 1
rs1056654
MPHOSPH6
0.925 0.160 16 82148406 3 prime UTR variant G/A snv 0.14 2
rs1056675
MPHOSPH6
0.925 0.160 16 82148329 3 prime UTR variant T/A;C snv 2
rs1064607
LPP
0.827 0.200 3 188877884 3 prime UTR variant G/C snv 0.46 5
rs11084377
FCAR
1.000 0.120 19 54875434 intron variant A/G;T snv 1
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs11102930
NGF-AS1 ; NGF
0.925 0.160 1 115338434 intron variant G/A snv 0.54 2
rs11150612 1.000 0.120 16 31346439 intergenic variant G/A snv 0.28 1
rs11150619
ITGAX
0.925 0.160 16 31365528 intron variant T/C snv 0.29 2
rs11264793
FCRL3
1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28 1
rs11264794
FCRL3
1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 2
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs1126616
SPP1
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs11574637
ITGAX
0.882 0.200 16 31357553 missense variant T/C snv 0.21 3
rs12022418
LOC105371664
1.000 0.120 1 192565977 intron variant C/A snv 0.64 1
rs12537
MTMR3 ; HORMAD2-AS1
0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4