Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs3087459
EDN1
0.925 0.160 6 12289406 upstream gene variant A/C snv 0.20 2
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
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
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs5070
APOA1 ; APOA1-AS
0.882 0.160 11 116837304 intron variant A/G snv 0.56 0.60 5
rs1187513719
CYP2C19
0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs243327
RMI2 ; LOC105371082
0.882 0.280 16 11259447 intron variant A/G snv 0.52 4
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4
rs2029253
ALOX5
0.925 0.200 10 45396036 intron variant A/G snv 0.37 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs2389995
HDAC9
0.925 0.200 7 18933395 intron variant A/G snv 6.0E-02 3
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs12766939
CUBN
0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs3784929
KARS1
0.925 0.160 16 75643129 intron variant A/G snv 0.30 2