Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6701752
LINC02768 ; LOC105373215
1 235939586 downstream gene variant G/A snv 0.93 1
rs1999537 1 56439852 intron variant G/A snv 0.89 2
rs11359909 3 128603031 intergenic variant G/- delins 0.89 4
rs6782812 3 128599154 intergenic variant G/A snv 0.89 1
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs163574
CNTN4 ; CNTN4-AS1
3 3055243 intron variant A/G snv 0.88 1
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs778798
FUT6
19 5839602 5 prime UTR variant A/C snv 0.82 1
rs1586068
IKZF2
2 213033508 intron variant A/G snv 0.81 2
rs301161
EMC8
16 85776743 intron variant G/A snv 0.81 2
rs3181077
CCR1 ; CCR3
1.000 0.080 3 46209161 intron variant C/T snv 0.80 1
rs7613595
PLCL2
3 16867007 intron variant C/A snv 0.79 2
rs2072735
SPSB1
1 9295413 intron variant A/C snv 0.76 2
rs4848100
ANAPC1
2 111630955 non coding transcript exon variant C/T snv 0.76 2
rs2335455
ELOB
16 2778172 non coding transcript exon variant T/C;G snv 0.74 2
rs511515
GGNBP1 ; BAK1
6 33573730 3 prime UTR variant A/G snv 0.73 2
rs2998286
LINC02652
10 28491444 intron variant T/C snv 0.73 5
rs2451279
LOC112267968
6 159094045 intron variant A/G snv 0.73 2
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs2251188 7 6664701 intron variant A/G snv 0.71 2
rs6427756
LINC01221
1 199031598 intron variant A/G snv 0.71 1
rs4449834
CHD7
8 60843309 intron variant G/T snv 0.71 2