Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11237982 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 1
rs12453507 0.925 0.200 17 39896954 intergenic variant C/G;T snv 1
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 1
rs12712133 1.000 0.080 2 102249813 downstream gene variant A/G snv 0.57 1
rs12936409 0.925 0.200 17 39887396 intergenic variant C/T snv 0.35 1
rs137603 1.000 0.080 22 39298220 downstream gene variant A/C snv 0.50 1
rs17033015 1.000 0.080 4 102625147 intergenic variant A/C snv 0.65 1
rs1859308 1.000 0.080 16 27386677 intergenic variant A/G snv 0.88 1
rs231725 0.851 0.240 2 203875952 downstream gene variant G/A snv 0.38 1
rs4675369 1.000 0.080 2 203778471 upstream gene variant A/G snv 0.15 1
rs4952108 1.000 0.080 2 30206869 upstream gene variant C/A;T snv 1
rs4973341 1.000 0.080 2 227795646 intergenic variant C/T snv 0.67 1
rs526231 1.000 0.080 5 103345680 intergenic variant C/T snv 0.24 1
rs6456156 0.925 0.200 6 167108812 intron variant T/C snv 0.46 1
rs6478106 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 1
rs6871748 1.000 0.080 5 35885880 intergenic variant T/C snv 0.21 1
rs77871618 1.000 0.080 11 118862915 intergenic variant C/T snv 6.6E-03 1
rs80065107 1.000 0.080 11 118812058 regulatory region variant T/C snv 1
rs10415976
ARID3A
1.000 0.080 19 941603 intron variant A/G snv 0.18 1
rs2550374
CCDC113
1.000 0.080 16 58220544 downstream gene variant G/T snv 0.70 1
rs510372
CCDC88B
1.000 0.080 11 64347665 intron variant C/A;T snv 1
rs12708715
CLEC16A
1.000 0.080 16 11083967 intron variant C/T snv 0.39 1
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 1
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 1
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 1