Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1
rs9999118
SPATA5
1.000 0.040 4 123130312 intron variant A/G snv 1.2E-02 1