Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 5
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 4
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 1
rs1329424
CFH
1.000 0.040 1 196677046 non coding transcript exon variant T/G snv 0.66 1
rs139161960 1.000 0.040 5 29538059 intergenic variant T/G snv 0.10 1
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 1
rs334353
TGFBR1
1.000 0.040 9 99146083 intron variant T/G snv 0.25 1
rs3750848
LOC105378525 ; ARMS2
1.000 0.040 10 122455799 intron variant T/G snv 0.23 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs74320127
HERC1
1.000 0.040 15 63782903 intron variant T/C;G snv 2
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 6
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs140647181
LOC105374007
0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs3750846
ARMS2 ; LOC105378525
0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs5754227
SYN3
0.851 0.040 22 32709831 intron variant T/C snv 0.26 4
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs10510110
PLEKHA1
0.925 0.120 10 122432914 3 prime UTR variant T/C snv 0.56 1
rs2071277
NOTCH4
0.882 0.200 6 32203906 intron variant T/C snv 0.48 0.46 1
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 1
rs422951
NOTCH4
0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 1