Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4
rs17035917
ARHGEF38
1.000 0.040 4 105599585 intron variant C/T snv 8.1E-02 2
rs11727735
INTS12 ; GSTCD
1.000 0.040 4 105710713 intron variant A/G snv 4.4E-02 2
rs76884941
LOC105374039 ; CD96
1.000 0.040 3 111482938 intron variant T/G snv 5.1E-02 1
rs56238310
LOC105374039 ; CD96
1.000 0.040 3 111514392 intron variant C/A;T snv 1
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 1
rs55645543
ANXA5
1.000 0.040 4 121686023 intron variant T/C;G snv 1
rs7068966
CDC123
1.000 0.040 10 12235993 intron variant C/T snv 0.43 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 1
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs10928927 1.000 0.040 2 129710793 intergenic variant C/T snv 0.70 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 2
rs9399401
ADGRG6
1.000 0.040 6 142347764 intron variant T/C snv 0.31 2
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 2
rs7697189
LOC105377462
1.000 0.040 4 144515742 intron variant G/A;C snv 2
rs1828591
LOC105377462
1.000 0.040 4 144559628 intron variant A/G snv 0.43 3
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 2
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 3
rs1512288 1.000 0.040 4 144570129 intron variant G/A snv 0.42 2
rs6817273 1.000 0.040 4 144570851 intron variant T/A;C snv 0.33 2
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 3
rs7689420
HHIP-AS1 ; HHIP
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 1