Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs12050217
BDKRB1
0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs10507875
OBI1-AS1 ; EDNRB
0.925 0.160 13 77943119 intron variant A/G snv 0.17 3
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs11018670 0.925 0.160 11 89623460 intergenic variant A/G snv 0.30 2
rs1571942
PLXDC2
0.925 0.160 10 20253705 intron variant A/G snv 0.15 2
rs6427247 0.925 0.160 1 170411339 regulatory region variant A/G snv 0.26 2
rs1057719
SLMAP
1.000 0.120 3 57927987 3 prime UTR variant A/G snv 0.31 1
rs11771617 1.000 0.120 7 125733372 intergenic variant A/G snv 0.20 1
rs1373054855
PECAM1
1.000 0.120 17 64370017 missense variant A/G snv 1.4E-05 1
rs148995025
LINC02196
1.000 0.120 5 7085094 intron variant A/G snv 8.9E-03 1
rs17376456
LOC105379087 ; KIAA0825
1.000 0.120 5 94221997 intron variant A/G snv 8.7E-02 1
rs17404956 1.000 0.120 5 166962488 regulatory region variant A/G snv 5.5E-02 1
rs2104455 1.000 0.120 6 9368285 intergenic variant A/G snv 0.30 1
rs3844492
ARHGAP22
1.000 0.120 10 48614756 intron variant A/G snv 0.38 1
rs39059
CHN2
1.000 0.120 7 29215854 intron variant A/G snv 0.32 1
rs4787008
RBFOX1
1.000 0.120 16 7365551 intron variant A/G snv 0.87 1
rs4885322
UCHL3
1.000 0.120 13 75597195 intron variant A/G snv 0.77 1
rs512825
LINC02774
1.000 0.120 1 244006892 intron variant A/G snv 0.39 1
rs779099001
WNK1
1.000 0.120 12 867971 missense variant A/G snv 4.0E-06 1
rs7982517
UCHL3
1.000 0.120 13 75587903 intron variant A/G snv 0.77 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12