Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs7975
GSTZ1
0.763 0.320 14 77326864 stop gained G/A;C;T snv 0.31 0.32 9
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs7832529
SLC20A2
0.882 0.120 8 42449295 intron variant T/C snv 0.24 3
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs779682021
CYP1A1
0.882 0.120 15 74721227 missense variant A/C snv 5
rs778990691
CCNH
0.807 0.240 5 87395069 missense variant A/G snv 4.0E-06 6
rs776223836
ERCC2
0.763 0.280 19 45364045 missense variant G/A snv 11
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 28
rs7727691
XRCC4 ; TMEM167A
0.763 0.200 5 83075876 intron variant C/T snv 0.32 9
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs771866347
GPX1
0.882 0.120 3 49358109 missense variant G/A snv 4.1E-06 3
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs765502022
UGT2B7
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs758057623
GSTP1
0.882 0.120 11 67584520 missense variant G/A snv 3
rs754554026
MLH1
0.827 0.160 3 37028864 missense variant G/A;C snv 2.8E-05 7.0E-06 5
rs744154
ERCC4
0.763 0.280 16 13921224 intron variant G/C snv 0.23 11