Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs113722913
LOC105371682
1 199950846 intergenic variant T/C snv 2.6E-02 3
rs2785980
LYPLAL1-AS1
1 219527177 intergenic variant T/C snv 0.28 3
rs6689335
LYPLAL1-AS1
1 219455340 intron variant T/C snv 0.31 3
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 1
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 1
rs1555543 1 96479241 intergenic variant A/C snv 0.55 1
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 1
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 1
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 1
rs516636 1 177886382 intron variant C/A snv 0.17 1
rs574367 1 177904075 intron variant G/T snv 0.16 1
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 4
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 3
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2