Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs73036519
EXOC3L2 ; MARK4
0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 5
rs10490924
ARMS2 ; LOC105378525
0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 4
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 4
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 4
rs11884770
COL4A3 ; MFF-DT
0.851 0.040 2 227222204 intron variant T/A;C snv 4
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 4
rs12357257
ARHGAP21
0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs140647181
LOC105374007
0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 4
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 4
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs181705462
CYP21A2 ; STK19
0.851 0.040 6 31979250 intron variant G/C;T snv 4
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 4
rs187328863
KCNT2
0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs191281603
CFHR5
0.851 0.040 1 196989521 intron variant C/G;T snv 4.6E-03 4
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 4