Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs28362930
SEMA7A
0.925 0.160 15 74408859 downstream gene variant G/A snv 0.16 3
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs9275424 6 32702799 downstream gene variant A/G snv 0.30 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs1888747
FRMD3
1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs3115573 1.000 0.120 6 32251066 upstream gene variant A/G snv 0.41 2
rs17880135
SCAF4
21 31669690 upstream gene variant T/G snv 3.9E-02 1
rs3764880
TLR8-AS1 ; TLR8
0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs1025423410
TLR1
4 38798831 start lost T/C snv 1
rs776400293
TLR3
4 186076620 start lost A/G snv 4.0E-06 7.0E-06 1
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs8731
GPN1 ; SUPT7L
2 27650459 3 prime UTR variant C/G snv 0.22 1
rs9932581
MVD ; CYBA
16 88651945 3 prime UTR variant C/T snv 0.39 1
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs8177412
GPX3 ; LOC105378228
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15 5
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14