Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs17635492 1.000 0.080 6 117450114 intron variant A/T snv 2.4E-02 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs55768116
MPZL3
0.925 0.080 11 118237616 intron variant C/A snv 0.38 2
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 2
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 1
rs1853837
FOXP4-AS1
1.000 0.080 6 41529297 intron variant C/A;T snv 1
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 1
rs55781567
CHRNA5
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 1
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 1
rs2868371
HSPB1
0.827 0.120 7 76301442 upstream gene variant C/G snv 0.22 1
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 11
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs1200399
BAZ1A
0.925 0.080 14 34823979 intron variant C/T snv 0.87 2
rs16950650
ABCC4
1.000 0.080 13 95123178 intron variant C/T snv 4.7E-02 2
rs3769821
CASP8
0.851 0.200 2 201258707 intron variant C/T snv 0.57 2
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs1209950 1.000 0.080 21 38801604 upstream gene variant C/T snv 0.30 1
rs12621220 1.000 0.080 2 112840678 non coding transcript exon variant C/T snv 0.24 1
rs1656402
EIF4E2
1.000 0.080 2 232561816 intron variant C/T snv 0.31 1
rs16893344
CCN4
0.807 0.160 8 133194036 intron variant C/T snv 0.29 1
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 1