Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs995343
SLC16A7
0.925 0.120 12 59685594 intron variant G/A snv 0.57 2
rs9927981
HP ; TXNL4B
1.000 0.080 16 72054753 non coding transcript exon variant C/T snv 1
rs9912773
STAT3
1.000 0.080 17 42358516 intron variant C/A;G snv 1
rs9909179 1.000 0.080 17 13140986 regulatory region variant T/C snv 0.37 1
rs984755949
COL11A2
1.000 0.080 6 33172302 missense variant A/C snv 1
rs979090956
ABCB1
0.827 0.200 7 87553822 missense variant G/C snv 5
rs9752
SFTPB
1.000 0.080 2 85659544 3 prime UTR variant G/C snv 0.46 1
rs969088 1.000 0.080 5 26389153 intron variant G/C snv 9.9E-02 1
rs967591
CD3EAP ; PPP1R13L
0.851 0.080 19 45406676 5 prime UTR variant G/A;C;T snv 0.22; 6.7E-06 4
rs9660710 1.000 0.080 1 1163962 upstream gene variant A/C;T snv 1
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs9642391
EGFR
1.000 0.080 7 55177671 intron variant G/C snv 0.24 1
rs9625921
HORMAD2
1.000 0.080 22 30112286 intron variant C/G snv 0.45 1
rs959173
CAV1
0.925 0.120 7 116542000 intron variant C/T snv 0.78 2
rs958335893
ALK
1.000 0.080 2 29193478 missense variant C/T snv 1
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs9535826
ATP7B
0.851 0.080 13 51991990 intron variant T/C;G snv 4
rs9526814
ATP7B
1.000 0.080 13 51965390 intron variant T/G snv 0.35 1
rs941759532
ERCC4
0.763 0.240 16 13932175 missense variant C/G snv 11
rs9390123
PHACTR2
1.000 0.080 6 143622177 intron variant T/C snv 0.60 1
rs938836
NOCT
1.000 0.080 4 139018499 intron variant G/A snv 0.42 1
rs937282
MDM2
1.000 0.080 12 68808017 upstream gene variant C/G snv 0.56 1
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs9295740 0.827 0.120 6 27721723 intergenic variant G/A snv 0.27 5