Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs10910845 0.925 0.120 1 145711946 upstream gene variant T/G snv 0.44 3
rs12129861
PDZK1
0.925 0.120 1 145709377 upstream gene variant C/T snv 0.43 3
rs1471633 0.925 0.120 1 145711327 upstream gene variant T/G snv 0.43 3
rs1539019
NLRP3
0.882 0.240 1 247436999 intron variant A/C snv 0.63 3
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 3
rs9728619
PDZK1
0.925 0.120 1 145698627 intron variant A/G snv 0.51 3
rs1023945
CD160
0.925 0.120 1 145731972 intron variant G/A snv 0.55 2
rs10752826
POLR3C
0.925 0.120 1 145832321 intron variant C/G snv 0.37 2
rs11264341
TRIM46
0.925 0.120 1 155179017 intron variant C/T snv 0.40 2
rs11587821
POLR3C
0.925 0.120 1 145836072 intron variant C/A;T snv 2
rs11591191
RNF115
0.925 0.120 1 145759132 intron variant A/G snv 0.29 2
rs12123298
RNF115
0.925 0.120 1 145744615 3 prime UTR variant G/A;C snv 0.27 2
rs12402867
RNF115
0.925 0.120 1 145798852 intron variant C/T snv 0.29 2
rs12405132
RNF115
0.882 0.200 1 145790097 intron variant G/A snv 0.29 2
rs12724816
RNF115
0.925 0.120 1 145795753 intron variant C/A snv 0.29 2
rs12750384
RNF115
0.925 0.120 1 145753588 intron variant A/G snv 0.28 2
rs1298954
PDZK1
0.925 0.120 1 145704906 intron variant C/T snv 0.44 2
rs1471628
CD160
0.925 0.120 1 145728029 intron variant A/T snv 0.55 2
rs17352469
RNF115
0.925 0.120 1 145741704 3 prime UTR variant T/C snv 0.28 2
rs17354678
RNF115
0.925 0.120 1 145745816 3 prime UTR variant T/C snv 0.30 2
rs2004659
NUDT17
0.925 0.120 1 145846884 intron variant A/G snv 0.30 2
rs2040086
RNF115
0.925 0.120 1 145783203 intron variant G/T snv 0.29 2
rs2231375
RNF115 ; CD160
0.925 0.120 1 145738392 3 prime UTR variant C/T snv 0.28 2
rs2318299
RNF115
0.925 0.120 1 145772412 non coding transcript exon variant A/G;T snv 2