Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs12362161 1.000 0.040 11 98834502 intergenic variant C/A;G snv 3
rs189919070
MIR4788
1.000 0.040 3 134436825 upstream gene variant C/A;T snv 3
rs7965830
LOC105369844
1.000 0.040 12 75962050 intron variant C/A;T snv 3
rs79661299 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 3
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 2
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 2
rs10519210 1.000 0.040 15 63445726 intergenic variant T/C;G snv 1
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 1
rs12638540
CMTM7
1.000 0.040 3 32447042 intron variant A/G;T snv 1
rs1520832 1.000 0.040 12 42859612 regulatory region variant T/C;G snv 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs548097 1.000 0.040 13 75202132 intergenic variant G/C;T snv 1
rs148133894 1.000 0.040 16 24584678 intergenic variant T/C snv 2.4E-03 3
rs149447933
LOC101928331 ; LOC105374942
1.000 0.040 6 14453908 intron variant C/G snv 4.4E-03 3