Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 5
rs11624776 14 93129246 regulatory region variant A/C;T snv 3
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 3
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 3
rs4804416
INSR
19 7223837 intron variant T/G snv 0.37 3
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 3
rs3813582
LINC01229 ; LOC105371356 ; MAFTRR
16 79715456 non coding transcript exon variant T/C snv 0.28 3
rs9472138
LOC107986598
0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 3
rs2046045
PDE8B
0.925 0.080 5 77239986 intron variant T/C;G snv 3
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 3
rs9497965
SASH1
1.000 0.040 6 148200156 regulatory region variant C/T snv 0.40 3
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 2
rs17776563 15 88575873 intergenic variant G/A;C snv 2
rs7240777 18 73500517 intergenic variant G/A snv 0.53 2
rs10519227
FAM227B ; FGF7
15 49454167 intron variant T/A snv 0.20 2
rs1571583
GLIS3
9 4267209 intron variant A/G snv 0.77 2
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 2
rs11755845
LINC01512
6 43937043 regulatory region variant C/T snv 0.21 2
rs13015993
LOC101928278
2 216760800 intron variant G/A snv 0.64 2
rs2396083
LOC105375069 ; LOC107986598
0.882 0.160 6 43837071 intron variant G/A;C;T snv 2
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 2
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 2
rs6499766
LPCAT2
16 55570216 intron variant A/T snv 0.54 2
rs334699
NFIA
1 61154824 intron variant A/G snv 0.92 2