Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003342
HORMAD2
22 30174033 intron variant A/G snv 0.45 1
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs10061469 5 73222321 intron variant T/C snv 0.37 1
rs10063949
SLC23A1
0.882 0.080 5 139383837 intron variant T/C snv 0.48 4
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 2
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 4
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs1020856343
SLC22A5
0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 5
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10486483
SKAP2
1.000 0.040 7 26852821 intron variant G/A snv 0.21 2
rs104895094
MEFV
0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs104895467
NOD2
0.851 0.120 16 50716899 missense variant A/G snv 1.2E-03 7.5E-04 5
rs10491434
IL7R
1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 2
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13 2
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs1051792
MICA
0.851 0.240 6 31411200 missense variant G/A snv 0.34 0.35 5
rs10521318 16 85977731 intron variant C/G;T snv 1
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11