Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95 3
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs2070995
KCNJ6-AS1 ; LOC107985507 ; KCNJ6
1.000 0.040 21 37714662 synonymous variant T/C snv 0.80 0.85 2
rs2562456
LINC00664
1.000 0.040 19 21483408 non coding transcript exon variant C/T snv 0.77 2
rs887200
ARVCF
22 19976143 intron variant C/T snv 0.74 1
rs1571138 1 46429969 upstream gene variant A/G snv 0.73 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs179971
ATXN1
6 16362511 intron variant C/T snv 0.66 1
rs4660928 1 46420268 TF binding site variant A/C snv 0.63 1
rs9524885
ABCC4
13 95283335 intron variant T/C snv 0.63 2
rs4587017
UGT2B7
4 69081680 intron variant T/G snv 0.63 1
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6276
DRD2
0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 8
rs2756109
ABCC2
10 99798989 intron variant G/T snv 0.53 1
rs398655 13 33013514 upstream gene variant A/C snv 0.51 1
rs7718461
CRHBP
5 76962223 intron variant A/G snv 0.51 1
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14