Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6581768
LOC105369816
12 67683408 intergenic variant A/G snv 0.25 1
rs6865647
PDE4D
5 59103374 intron variant A/G;T snv 1
rs7195832 16 19947804 intergenic variant T/A snv 1
rs751772105
KCNJ11
11 17387362 missense variant C/A;T snv 4.0E-05 1
rs762533455
ADRB2
5 148827300 missense variant G/A snv 4.0E-06 1
rs770069803
PDE4D
5 58977286 missense variant C/G snv 4.0E-06 1
rs775077692
CETP
16 56963027 missense variant A/C;G snv 4.0E-06; 4.0E-06 1
rs7784820
CD36
7 80420717 intron variant A/G snv 0.16 1
rs78351985
C4orf54
4 99655532 upstream gene variant A/G snv 3.2E-04 1
rs883484 9 122362748 intergenic variant C/T snv 0.20 1
rs9658625
SOAT2
12 53103618 missense variant A/G snv 9.3E-02 7.4E-02 1
rs996876302
PECAM1
17 64363155 missense variant C/T snv 3.5E-05 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134