Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs12373124
SPPL2C ; MAPT-AS1
0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 3
rs201563 0.807 0.080 20 22019643 intergenic variant C/T snv 0.49 1
rs2180439 0.807 0.080 20 21872462 intergenic variant C/T snv 0.58 1
rs2497938 0.807 0.080 X 67343176 intergenic variant T/C snv 0.37 1
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 1
rs6625163 0.807 0.080 X 67291142 intergenic variant G/A snv 0.62 1
rs9287638 0.807 0.080 2 238785990 downstream gene variant C/A snv 0.40 1
rs12565727
C1orf127
0.807 0.080 1 10973025 intron variant A/G snv 0.31 1
rs2073963
HDAC9
0.807 0.080 7 18838251 intron variant T/G snv 0.43 1
rs1160312
LINC01432
0.807 0.080 20 22069865 intron variant A/G snv 0.55 1
rs6047844
LINC01432
0.807 0.080 20 22056937 intron variant T/C snv 0.54 1
rs6945541
LOC105375343
0.807 0.080 7 69146973 intron variant C/T snv 0.68 1
rs919462
MAPT
0.807 0.120 17 45988374 intron variant C/T snv 0.15 1
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32 1
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv 1