Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 2
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs3917265
IL1R1
1.000 0.120 2 102162001 intron variant T/C snv 0.50 2
rs45616239
KIAA1109
0.925 0.120 4 122335010 intron variant T/C snv 0.13 2
rs17690965
KIF3A
0.925 0.160 5 132694975 3 prime UTR variant C/G snv 0.57 2
rs4705962
KIF3A
0.925 0.160 5 132693166 3 prime UTR variant T/A;C snv 2
rs9405490
LOC102723944
0.925 0.120 6 1510423 downstream gene variant G/A snv 0.20 2
rs993226
LOC105369875
0.851 0.160 12 84492794 intergenic variant T/G snv 6.3E-02 2
rs4363385
LOC105371446
0.925 0.120 1 153016845 upstream gene variant T/C snv 0.62 2
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2
rs80312298
MGMT
0.925 0.120 10 129683009 intron variant C/A;T snv 2
rs2251396
MICA-AS1
0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 2
rs6548123
MYT1L
0.925 0.120 2 2221629 intron variant C/T snv 0.76 2
rs62176107
PRKRA ; CHROMR
0.925 0.120 2 178436244 missense variant G/A;T snv 2
rs2533291
PTPRN2
0.925 0.120 7 157712962 intron variant C/T snv 0.12 2
rs6596086
RAD50
0.925 0.120 5 132616530 intron variant T/C snv 0.34 2
rs380743
RASIP1
0.925 0.120 19 48737757 intron variant G/A;C snv 2
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 2
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs6684514
TMEM79 ; SMG5
0.925 0.120 1 156285665 missense variant G/A snv 0.27 0.24 2
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2