Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 2
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 2
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 2
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 2
rs1570669
CYP24A1
0.925 0.080 20 54157888 intron variant A/G snv 0.42 2
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 2
rs1978503
LINC01416 ; LOC107985164
0.882 0.160 18 55997051 non coding transcript exon variant A/G snv 0.18 2
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 2
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 2
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 2
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 1
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 1
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 1
rs12443621
TOX3
0.807 0.120 16 52514125 intron variant A/G snv 0.48 1
rs1265507
LOC105369998
0.925 0.080 12 114430333 regulatory region variant A/G snv 0.52 1
rs1292011
LOC105370003
0.851 0.080 12 115398717 regulatory region variant A/G snv 0.43 1
rs13329835
CDYL2
0.925 0.080 16 80616908 intron variant A/G snv 0.35 1
rs17435444
TNIP3
0.925 0.080 4 121200339 intron variant A/G snv 4.8E-02 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs2227928
ATR
0.851 0.200 3 142562770 missense variant A/G snv 0.55 0.63 1