Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 5
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 5
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs9295684 0.925 0.120 6 26069441 intergenic variant T/C snv 0.38 5
rs9358901 0.925 0.120 6 26024208 downstream gene variant G/T snv 0.67 5
rs9379818 0.925 0.120 6 26022978 downstream gene variant G/A;T snv 5
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 5
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 5
rs6976930
BAZ1B
0.925 0.120 7 73471480 intron variant G/A snv 0.23 5
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 5
rs10208529
C2orf16
0.925 0.120 2 27563321 intron variant A/T snv 0.28 5
rs4665382
C2orf16
0.925 0.120 2 27560934 intron variant T/C snv 0.23 5
rs4665383
C2orf16
0.925 0.120 2 27568688 synonymous variant C/G snv 0.24 5