Source: GWASDB ×
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 5
rs17646665
SORT1
1.000 0.080 1 109369429 intron variant A/G snv 5.8E-02 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 3
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs12091371
FMN2
1.000 0.080 1 240441752 intron variant G/A snv 0.18 1
rs1408077
CR1
1.000 0.080 1 207630796 intron variant A/C snv 0.84 1
rs1408078
CR1
1.000 0.080 1 207627210 intron variant T/C snv 0.84 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2296160
CR1
0.925 0.120 1 207621975 missense variant A/G snv 0.82 0.81 1
rs2421847
PRRC2C
1.000 0.080 1 171588461 missense variant A/G snv 3.3E-02 2.8E-02 1
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 1
rs4145462
MPZL1
1.000 0.080 1 167749262 intron variant A/G;T snv 1
rs4844610
CR1
1.000 0.080 1 207629207 intron variant A/C snv 0.87 1
rs4907035
LINC01725
1.000 0.080 1 83649216 intron variant A/T snv 0.43 1
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 1
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 1
rs6678275 1.000 0.080 1 193656103 intron variant G/C;T snv 1
rs6701713
CR1
1.000 0.080 1 207612944 intron variant A/G;T snv 1
rs7539409
LINC01725
1.000 0.080 1 83789052 intron variant G/A snv 0.90 1
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 2