Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs35610040
CST3
1.000 0.040 20 23635832 intron variant T/C snv 0.19 2
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 2
rs16985615
LOC107985383
1.000 0.040 20 23661790 intron variant T/A;C snv 2
rs1158167 20 23597552 downstream gene variant G/A snv 0.72 1
rs2424590 20 23656343 non coding transcript exon variant C/T snv 0.83 1
rs6036478
CST3
20 23630722 intron variant C/A snv 0.21 1