Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs1718125
LOC105370032 ; P2RX7
0.851 0.200 12 121155216 intron variant C/T snv 0.15 0.19 6
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs16868943
COL11A2
1.000 0.040 6 33179950 intron variant G/A snv 2.9E-02 3
rs2835859
KCNJ6
0.925 0.200 21 37645860 intron variant T/C snv 0.16 3
rs3845446
CACNA1E
1 181797301 intron variant T/C snv 6.3E-02 3
rs7016778
OPRK1
8 53237545 intron variant A/T snv 0.17 3
rs740603
COMT
0.925 0.040 22 19957654 intron variant A/G snv 0.48 3
rs13080116
SCN11A
3 38865732 intron variant T/C snv 0.23 2
rs1972597 1.000 0.040 17 77598082 intron variant T/C snv 0.31 2
rs2817040
LOC285847 ; ARMC12
6 35737829 intron variant G/A snv 0.22 2