Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10051924
IRGM
1.000 0.040 5 150847077 5 prime UTR variant T/C snv 0.21 1
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs1017281
ASAP1
1.000 0.040 8 130234967 intron variant G/A snv 0.37 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1041983
NAT2
0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 15
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1045481
GEMIN4
1.000 0.040 17 744917 missense variant G/A;C snv 0.20 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs10500804
CYP2R1
0.925 0.040 11 14888727 intron variant T/G snv 0.35 2
rs10507172
HSP90B1 ; C12orf73
1.000 0.040 12 103949490 intron variant G/A snv 7.2E-02 1
rs10507173
HSP90B1 ; C12orf73
1.000 0.040 12 103950058 intron variant A/G snv 6.3E-02 1
rs10514611
IRF8
0.925 0.080 16 85921636 3 prime UTR variant C/T snv 0.23 2
rs1052632
MR1
0.925 0.080 1 181051094 non coding transcript exon variant G/A;C snv 2
rs1052677
POLD1 ; NR1H2
1.000 0.040 19 50382924 3 prime UTR variant C/G;T snv 0.45 1
rs1055229
LINC01857
1.000 0.040 2 207666959 non coding transcript exon variant C/T snv 0.26 2
rs1059225
SFTPA1
1.000 0.040 10 79615230 3 prime UTR variant T/C snv 0.47 1
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs1075309 1.000 0.040 2 5113465 intergenic variant C/T snv 0.20 1
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10766197
CYP2R1
0.807 0.240 11 14900334 upstream gene variant G/A;C snv 6
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14