Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 4
rs130154
TAFA5
1.000 0.040 22 48710770 intron variant C/T snv 0.69 1
rs7903456
SHLD2
0.882 0.160 10 87159562 intron variant C/T snv 0.69 3
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs893006
SLC22A12
0.882 0.160 11 64598324 intron variant C/A snv 0.61 3
rs1822825
PPARG
0.925 0.080 3 12408464 intron variant G/A snv 0.61 2
rs2941484
HNF4G
0.882 0.160 8 75566533 3 prime UTR variant C/T snv 0.52 4
rs3825016
SLC22A12
0.882 0.160 11 64591814 synonymous variant C/T snv 0.57 0.51 3
rs11231825
SLC22A12
0.827 0.240 11 64592802 synonymous variant T/C snv 0.57 0.51 5
rs11602903
SLC22A12
0.882 0.120 11 64590769 5 prime UTR variant A/T snv 0.51 3
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs505802
SLC22A12
0.882 0.160 11 64589600 upstream gene variant T/C snv 0.45 4
rs559946
SLC22A12
1.000 0.040 11 64591133 5 prime UTR variant T/C snv 0.45 1
rs2544390
LRP2
0.925 0.080 2 169348336 intron variant C/T snv 0.45 4
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs7688672
PRKG2
0.925 0.160 4 81148295 intron variant G/A snv 0.39 2
rs12218
SAA1
0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs7929627
SLC22A12
1.000 0.040 11 64600264 intron variant A/G snv 0.34 1
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 7
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs475688
SLC22A12
0.882 0.160 11 64596819 intron variant C/T snv 0.25 3
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65