Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2285053
MMP2
0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs7194256
SLC6A2
0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 7
rs12817819
ATP2B1
0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02 3
rs1334067073
ACE
0.925 0.120 17 63478025 missense variant C/G;T snv 4.2E-06 2
rs1799979
SCNN1B
1.000 0.040 16 23380659 missense variant C/G;T snv 8.1E-06; 2.1E-03 2
rs11749255 1.000 0.040 5 174642665 intergenic variant A/G snv 0.28 1
rs6487504 1.000 0.040 12 25654374 regulatory region variant C/G;T snv 1
rs324498
PTPRD
1.000 0.040 9 9059545 intron variant G/A snv 0.70 1