Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1017119
C5
1.000 0.080 9 121045260 intron variant T/C snv 2.0E-02 1
rs10204475
UBR3
1.000 0.080 2 170076012 intron variant T/G snv 0.78 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10400694 1.000 0.080 14 84147550 intergenic variant G/C;T snv 1
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs10431036
BCO2
1.000 0.080 11 112176338 5 prime UTR variant G/A snv 0.11 1
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2
rs1044925
SOAT1
0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10487667
TBXAS1
1.000 0.080 7 139984244 intron variant T/A;G snv 1
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051922
IFNB1
1.000 0.080 9 21077717 synonymous variant G/A snv 0.33 0.35 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052053
PMF1 ; PMF1-BGLAP
1.000 0.080 1 156232382 missense variant A/C;G snv 1.0E-03; 0.38 3
rs1057293
SGK1
0.925 0.120 6 134172259 synonymous variant G/A snv 0.12 0.11 4
rs1057335
SERPINF2
0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5