Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 1
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 3
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 2
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 1
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 1
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 1
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 1
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 7
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 2