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
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs121907892
SLC22A12
0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs1451506414
SLC22A12
0.882 0.200 11 64598561 synonymous variant G/A snv 4
rs1370328347
CSH1
1.000 0.080 17 63895621 missense variant C/A;T snv 1.0E-05; 1.0E-05 1
rs767816037
CSH2
1.000 0.080 17 63872725 missense variant C/G;T snv 4.5E-05 1
rs775020499
LRSAM1
1.000 0.080 9 127467764 missense variant A/G snv 8.2E-06 1
rs782818582
ADAMTS13
0.882 0.160 9 133456116 stop gained C/T snv 1.2E-05 7.0E-06 3
rs753482595
SLC2A9
0.925 0.200 4 9920389 missense variant T/C snv 8.0E-06 1.4E-05 3
rs121907896
SLC22A12
0.851 0.200 11 64591825 missense variant G/A snv 1.8E-04 8.4E-05 5
rs561633150
SLC2A9
0.925 0.200 4 9980627 missense variant C/T snv 6.1E-04 9.1E-05 2
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2276415
AQP11 ; CLNS1A
0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs2233417
NFKBIA
1.000 0.080 14 35402888 intron variant C/T snv 0.14 0.13 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1955656
SERPINA5
1.000 0.080 14 94579038 intron variant G/A snv 0.14 1
rs2093266
SERPINA5 ; SERPINA4
1.000 0.080 14 94566450 intron variant G/A snv 0.15 1
rs1050851
NFKBIA
1.000 0.080 14 35403720 synonymous variant G/A snv 0.17 0.15 1
rs8094315
BCL2
1.000 0.080 18 63268814 intron variant A/G snv 0.17 1
rs62341657 1.000 0.080 4 184238385 intergenic variant G/A snv 0.18 1
rs10854554 0.925 0.080 22 19623159 regulatory region variant A/G snv 0.18 2
rs62341639 0.925 0.080 4 184238281 intergenic variant C/T snv 0.20 2