Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1048101
ADRA1A
0.882 0.120 8 26770511 missense variant A/G snv 0.52 0.56 5
rs104886142
COL4A5
0.790 0.280 X 108598793 missense variant G/A snv 8.7E-05 4.7E-05 10
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 4
rs104893914
NR3C1
1.000 0.080 5 143282714 missense variant C/T snv 2
rs104894145
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.925 0.240 10 102830946 missense variant G/A snv 3
rs10491093 17 10978681 intergenic variant T/G snv 0.72 1
rs10491334
CAMK4
5 111436706 intron variant C/T snv 0.14 1
rs1049331
LOC105378525 ; HTRA1
0.851 0.040 10 122461754 synonymous variant C/T snv 0.32 0.23 5
rs10496288 2 83065441 intergenic variant T/C snv 0.13 1
rs10496289 2 83066256 intergenic variant C/T snv 0.13 1
rs10501367
APLNR
1.000 0.040 11 57238113 upstream gene variant T/C snv 0.73 2
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1050606
ANXA5
1.000 0.080 4 121696891 5 prime UTR variant A/C snv 0.50 2
rs10509676
CYP2C19
10 94763288 intron variant A/G;T snv 0.16 1
rs10509681
CYP2C8
0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 8
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs10519963
NR3C2
4 148376523 intron variant G/A snv 0.12 1
rs10520097
LPIN1
2 11793260 intron variant A/G snv 0.12 1
rs1054889
XDH
2 31334442 3 prime UTR variant G/A snv 0.40 1
rs1057293
SGK1
0.925 0.120 6 134172259 synonymous variant G/A snv 0.12 0.11 4
rs1057518797
PKD2
4 88008090 frameshift variant CCCGGGCA/TAGGACG delins 3