Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 5
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 4
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 3
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3