Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs12185233
SPPL2C ; MAPT-AS1
0.882 0.160 17 45846288 missense variant G/A;C snv 9.5E-05; 0.15 4
rs12373142
SPPL2C ; MAPT-AS1
0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 3
rs566672630
KANSL1
0.925 0.120 17 46171403 missense variant T/A;C snv 3
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs1052594
MAPT
1.000 0.080 17 46025323 3 prime UTR variant G/A;C snv 2
rs1076222
KANSL1
1.000 0.080 17 46032403 non coding transcript exon variant C/G;T snv 2
rs11079729
KANSL1
1.000 0.080 17 46038203 non coding transcript exon variant C/A;T snv 2
rs12150090
KANSL1
1.000 0.080 17 46038520 non coding transcript exon variant C/G;T snv 8.0E-06; 0.14 2
rs12150447
KANSL1
1.000 0.080 17 46050759 intron variant A/C;G snv 2
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs17652449
MAPT
1.000 0.080 17 46011571 intron variant G/A;C snv 2
rs17652502
MAPT
1.000 0.080 17 46017105 intron variant G/A;T snv 2
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 2
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 2
rs2942167
LINC02210-CRHR1 ; LINC02210
1.000 0.080 17 45637652 non coding transcript exon variant T/A;C snv 2
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 2
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 2
rs7503377
CDK12
1.000 0.080 17 39552588 intron variant T/C;G snv 2