Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 2
rs1555543 1 96479241 intergenic variant A/C snv 0.55 2
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 2
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 2
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 2
rs516636 1 177886382 intron variant C/A snv 0.17 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs574367 1 177904075 intron variant G/T snv 0.16 2
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 2
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 1
rs11264483
C1orf61
1 156436589 intron variant G/C snv 0.45 1
rs1514174
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74527379 intron variant C/T snv 0.44 1
rs1514177
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.080 1 74525718 intron variant C/G snv 0.49 1
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 1
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs518785 1 110817180 regulatory region variant G/A snv 0.82 1
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 1
rs7534091 1 118321993 intergenic variant A/G snv 0.23 1