Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5
rs676457
ABO
1.000 0.120 9 133270797 intron variant T/A snv 3
rs6141803 1.000 0.120 20 32752550 TF binding site variant T/C snv 0.13 2
rs11086998
CD40
1.000 0.120 20 46128885 missense variant C/G;T snv 2.2E-02 1
rs1208732776
THPO ; CHRD
1.000 0.120 3 184378252 missense variant G/A snv 7.0E-06 1
rs4661012
PEAR1
1.000 0.120 1 156915699 3 prime UTR variant T/G snv 0.36 1
rs5369
EDN1
1.000 0.120 6 12294025 synonymous variant A/G snv 0.90 0.88 1
rs580253
CASP1
1.000 0.120 11 105029761 synonymous variant G/A snv 0.17 0.15 1
rs9508835
ALOX5AP
1.000 0.120 13 30760561 intron variant C/A snv 0.23 1
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 8
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 7
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs2075252
LRP2
0.925 0.160 2 169154475 stop gained T/A;C snv 0.76 5
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs5070
APOA1 ; APOA1-AS
0.882 0.160 11 116837304 intron variant A/G snv 0.56 0.60 5
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs822442
PEAR1
0.851 0.160 1 156913423 missense variant C/A;T snv 0.14; 4.0E-06 4
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs2762939
CYP24A1
0.925 0.160 20 54164712 intron variant G/C;T snv 3
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs3737224
PEAR1
0.882 0.160 1 156909788 synonymous variant C/T snv 0.14 0.13 3
rs41273215
PEAR1
0.882 0.160 1 156912167 intron variant C/T snv 0.13 3
rs12766939
CUBN
0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs3087459
EDN1
0.925 0.160 6 12289406 upstream gene variant A/C snv 0.20 2