Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1326934
SORBS1
0.925 0.200 10 95524324 intron variant C/T snv 0.63 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10868025
FRMD3
1.000 0.120 9 83549261 intergenic variant A/G snv 0.30 1
rs1888747
FRMD3
1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs1056534
FN3K ; TBCD
0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs9674559
RPTOR
0.925 0.160 17 80741808 intron variant A/G snv 0.22 2
rs7211818
RPTOR
0.827 0.200 17 80715103 intron variant A/G snv 0.23 5
rs7212142
RPTOR
0.827 0.200 17 80650141 intron variant G/A snv 0.50 5
rs1298908
LOC100130698
1.000 0.120 10 80253378 non coding transcript exon variant C/T snv 0.48 0.53 1
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs11107616
NAV3
1.000 0.120 12 77971000 intron variant T/G snv 0.13 1
rs2346061
CNDP1
1.000 0.120 18 74533297 upstream gene variant C/A snv 0.71 1
rs7577
CNDP2
1.000 0.120 18 74521112 3 prime UTR variant T/A;C;G snv 0.21 1
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs117897666
LOC105370892
0.882 0.160 15 73811619 intergenic variant C/T snv 3
rs58624704
ALB
0.925 0.200 4 73410325 missense variant G/A snv 8.0E-06 3.5E-05 2
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs11538209
ALB
1.000 0.120 4 73404356 missense variant T/C snv 2
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7