Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 1
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 1
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 2
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 2
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 3
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 1
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 2
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 1
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 1
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 3