Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1723018
CD247
1.000 0.080 1 167464183 intron variant A/G snv 0.33 1
rs2147959
H2BU1
1.000 0.080 1 228456531 upstream gene variant A/T snv 0.84 1
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 1
rs2786098
CRB1
1.000 0.080 1 197356778 intron variant T/A;G snv 1
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 1
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 1
rs301816
RERE
1.000 0.080 1 8444998 intron variant G/A snv 0.55 1
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 1
rs3828058
RORC
1.000 0.080 1 151813805 non coding transcript exon variant G/A snv 0.31 1
rs4233366
ADAMTS4
1.000 0.080 1 161189357 3 prime UTR variant C/T snv 0.32 1
rs4845774 1.000 0.080 1 152473145 intergenic variant T/C snv 0.57 1
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 1
rs541559418
TDRKH
1.000 0.080 1 151788046 intron variant G/A;C snv 1
rs646356
MROH7-TTC4 ; MROH7
1.000 0.080 1 54702100 missense variant T/A snv 0.87 0.89 1
rs662064
PEX14
1.000 0.080 1 10497194 intron variant T/C snv 0.66 1
rs6683383
ADORA1
1.000 0.080 1 203131376 intron variant T/A snv 0.25 1
rs6691738 1.000 0.080 1 173182897 downstream gene variant T/G snv 0.44 1
rs72702900 1.000 0.080 1 152799487 downstream gene variant T/A snv 2.3E-02 1
rs7517302
RUNX3
1.000 0.080 1 24927826 intron variant C/T snv 0.53 1
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 1
rs7551641 1.000 0.080 1 119475304 downstream gene variant A/C snv 6.6E-02 1
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 1
rs946261 1.000 0.080 1 203188745 upstream gene variant C/T snv 0.47 1
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7