Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs9838915
KLF15
0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs189919070
MIR4788
1.000 0.040 3 134436825 upstream gene variant C/A;T snv 3
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs4528684 1.000 0.040 19 14240762 intergenic variant C/T snv 0.12 1
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs139130723 1.000 0.040 6 14411553 intergenic variant A/G snv 4.4E-03 3
rs142803096 1.000 0.040 6 14420151 intergenic variant G/C snv 4.4E-03 3
rs149447933
LOC101928331 ; LOC105374942
1.000 0.040 6 14453908 intron variant C/G snv 4.4E-03 3
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs1258130495
EDNRA
0.882 0.040 4 147485727 missense variant G/A snv 3
rs899115126
EDNRA
0.882 0.080 4 147542603 missense variant G/C snv 3
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246