Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10007052
RNF150
1.000 0.040 4 141084419 intron variant C/A snv 0.31 1
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10013495 1.000 0.040 4 144584486 intron variant C/T snv 0.23 1
rs1002149
GSR ; UBXN8
1.000 0.040 8 30728221 upstream gene variant G/T snv 0.20 1
rs10023464 1.000 0.040 4 68794020 intergenic variant C/T snv 0.15 2
rs10037493
LOC107986462 ; HTR4
1.000 0.040 5 148475407 intron variant C/G;T snv 1
rs10056066
SGCD
1.000 0.040 5 156434616 intron variant G/A snv 2.4E-02 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10076733
IRF1-AS1 ; LINC02863
1.000 0.040 5 132425039 intron variant G/T snv 0.17 1
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs10114763
GLIS3
1.000 0.040 9 4143749 intron variant A/T snv 0.39 1
rs10152300
ADAMTSL3
1.000 0.040 15 83724155 intron variant G/A snv 0.84 1
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs10279301
LINC01006
1.000 0.040 7 156468621 intron variant C/T snv 0.14 1
rs1038376
CYP2B6
1.000 0.040 19 41018104 3 prime UTR variant A/T snv 0.31 1
rs1042711
ADRB2
0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
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
rs10429950 1.000 0.040 1 218451191 intergenic variant T/C snv 0.33 3
rs1043618
HSPA1L ; HSPA1A
0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs10439273
SPAG16
1.000 0.040 2 214283391 intron variant A/G snv 0.16 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10465586
CFH
1.000 0.040 1 196718199 intron variant A/T snv 0.44 2
rs10476890
SPINK14
1.000 0.040 5 148168700 intron variant G/A snv 0.10 2
rs1048290
KEAP1
0.851 0.160 19 10489766 synonymous variant G/C snv 0.41 0.48 4