Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1050606
ANXA5
1.000 0.080 4 121696891 5 prime UTR variant A/C snv 0.50 2
rs9402349
ENPP1
1.000 0.080 6 131863968 intron variant A/C snv 9.8E-02 1
rs2278239
CMYA5
1.000 0.080 5 79737483 missense variant A/C;G snv 0.14; 2.8E-05 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs75404003
TNFRSF11A
1.000 0.080 18 62361277 intron variant C/- delins 1
rs2960321
RYR1
1.000 0.080 19 38557523 intron variant C/A snv 0.18 1
rs201278114
MYBPC3
0.925 0.120 11 47352635 missense variant C/A;G snv 4.3E-06; 3.0E-04 3
rs238234
CAMTA2
1.000 0.080 17 4980523 missense variant C/A;G;T snv 5.6E-05; 0.75; 8.1E-06 1
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1178625972
GRAP2
1.000 0.080 22 39966117 missense variant C/G snv 2.4E-05 1.4E-05 1
rs2296545
LIPJ ; RNLS
0.851 0.160 10 88583080 missense variant C/G;T snv 0.46 8
rs4966014
IGF1R
0.882 0.200 15 98704789 intron variant C/G;T snv 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23