Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs1323292
LOC105371664
0.882 0.160 1 192571891 intron variant G/A snv 0.86 3
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 3
rs6662618 0.882 0.200 1 92469854 downstream gene variant T/G snv 0.75 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 3
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 2
rs1359062
LOC105371664
0.925 0.160 1 192572342 intron variant C/A;G;T snv 2
rs17519972
GLMN ; RPAP2
1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs2205986
SYT14
0.925 0.160 1 209942767 intron variant G/A snv 0.92 2
rs2300747
MIR548AC ; CD58
0.882 0.200 1 116561593 intron variant A/G snv 0.19 2
rs35967351
SLAMF7
1.000 0.080 1 160742014 intron variant A/T snv 0.26 2
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 2
rs666930
PHGDH
0.925 0.160 1 119716347 intron variant T/A;C snv 2