Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs1060499680
GNPTAB
0.882 0.200 12 101768036 splice donor variant C/A;T snv 4.0E-06 6
rs1337185
COL11A1
0.851 0.160 1 103079209 intron variant C/G;T snv 0.15 5
rs162509
ADAMTS5 ; MIR4759
0.925 0.160 21 26953456 intron variant C/A;G snv 3
rs2234677
IL1RN
2 113117932 5 prime UTR variant G/A;T snv 2