Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3018362 0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67 3
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs10494112 0.925 0.080 1 109809855 downstream gene variant A/G snv 0.17 2
rs2957128 0.925 0.080 18 62393502 downstream gene variant A/G snv 0.56 2
rs2980996 0.925 0.080 18 62311902 downstream gene variant C/G;T snv 2
rs484959 0.882 0.120 1 109823461 upstream gene variant T/A;C snv 2
rs499345 0.925 0.080 1 109819060 intergenic variant C/A snv 0.32 2
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 2
rs2458413
DCSTAMP ; DPYS
0.925 0.080 8 104347204 intron variant C/T snv 0.44 2
rs4294134
NUP205
0.925 0.080 7 135608380 intron variant A/G snv 0.76 2
rs1561570
OPTN
0.925 0.080 10 13113726 intron variant T/C snv 0.43 2
rs825411
OPTN
0.925 0.080 10 13127374 intron variant A/G;T snv 2
rs4941107
PIGN
0.925 0.080 18 62084098 intron variant A/G snv 0.58 2
rs663354
PIGN
0.925 0.080 18 62087057 intron variant C/T snv 0.25 2
rs9636100
PIGN
0.925 0.080 18 62044077 3 prime UTR variant A/G snv 0.51 2
rs10498635
RIN3
0.925 0.080 14 92636964 intron variant C/T snv 0.14 2
rs5910578
SLC25A43
0.925 0.080 X 119433739 intron variant T/A;C;G snv 2
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1