Source: GWASCAT

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 1
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
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 2
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 2
rs10486483
SKAP2
1.000 0.040 7 26852821 intron variant G/A snv 0.21 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
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 1
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
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
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10798069
PLA2G4A
1.000 0.040 1 186906327 intron variant G/T snv 0.37 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10896794
LPXN
11 58571651 intron variant T/C snv 0.19 1
rs10956252
LOC105375746
8 125523895 intron variant C/G;T snv 1
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3