Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs7704116
PPP2CA
1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 2
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs375752214
NOS3
0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs8177412
GPX3 ; LOC105378228
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15 5
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs140511594
TTC21B ; TTC21B-AS1
0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs4972593
LOC107985961
0.925 0.200 2 173598126 intergenic variant T/A snv 0.20 3
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs869025495
NPHS2
0.851 0.080 1 179564715 missense variant G/A snv 6
rs776400293
TLR3
4 186076620 start lost A/G snv 4.0E-06 7.0E-06 1
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs55807605
CFH
1 196736919 missense variant G/A snv 1.4E-03 5.5E-04 1
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs57960694
CFHR5
1 196994083 missense variant G/A snv 1.1E-02 3.6E-02 1
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11