Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 5
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs4575098
ADAMTS4 ; B4GALT3
1.000 0.080 1 161185602 3 prime UTR variant G/A snv 0.18 2
rs72639058
KAZN
1.000 0.080 1 13913797 intron variant C/A;T snv 2
rs823118 0.925 0.080 1 205754444 upstream gene variant C/A;T snv 2
rs11118328
CR1L
1.000 0.080 1 207677194 intron variant C/T snv 0.86 1
rs11588387
AHCYL1
1.000 0.080 1 109995242 intron variant C/T snv 6.0E-02 1
rs12036785
CR1
1.000 0.080 1 207619564 intron variant C/A snv 0.47 1
rs12041233 1.000 0.080 1 37287106 intron variant G/A snv 6.6E-02 1
rs12091371
FMN2
1.000 0.080 1 240441752 intron variant G/A snv 0.18 1
rs12752888
LINC02784
0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 1
rs137929838
COLGALT2
1.000 0.080 1 183941302 intron variant G/T snv 8.5E-03 1
rs143083071 1.000 0.080 1 99242198 intron variant G/A snv 3.1E-03 1
rs181424343
TGFB2
1.000 0.080 1 218421142 intron variant G/A snv 7.2E-03 1
rs182798940
SZT2 ; HYI
1.000 0.080 1 43453815 5 prime UTR variant C/A;T snv 8.9E-02 1
rs186911969 1.000 0.080 1 17877570 intergenic variant C/T snv 1
rs2093760
CR1
1.000 0.080 1 207613483 intron variant A/G snv 0.74 1
rs2243170
IL19
1.000 0.080 1 206836565 intron variant T/C snv 0.84 1
rs2421847
PRRC2C
1.000 0.080 1 171588461 missense variant A/G snv 3.3E-02 2.8E-02 1