Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28451617
ZSCAN25 ; CYP3A7-CYP3A51P ; CYP3A7
0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805018
PLA2G7
0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 6
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs516651
EGLN1
1.000 0.040 1 231406910 intron variant C/T snv 0.15 1
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs2515475
ANGPT2 ; MCPH1
1.000 0.040 8 6530918 intron variant C/T snv 0.19 1
rs10905928
CELF2
1.000 0.040 10 11300924 intron variant C/A snv 0.21 1
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs1965708
SFTPA2
0.851 0.200 10 79557289 missense variant G/T snv 0.22 0.25 6
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs2592178
C2orf42 ; TIA1
1.000 0.040 2 70245350 intron variant G/A snv 0.27 1
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3848719
ZNF335
1.000 0.040 20 45967906 synonymous variant G/A snv 0.33 0.32 1
rs3814634
CELF2 ; CELF2-AS2
1.000 0.040 10 11099442 splice region variant G/T snv 0.37 1
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs9605146
XKR3
1.000 0.040 22 16784304 missense variant G/A snv 0.39 1