Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs192427471 0.925 0.040 4 124644124 intergenic variant C/T snv 2.4E-03 2
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
rs149232047 0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04 2
rs16999497 0.925 0.040 X 129601222 regulatory region variant T/C snv 7.8E-02 2
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02 2
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs12566888
PEAR1
0.807 0.280 1 156899255 intron variant G/T snv 0.26 7
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
rs822442
PEAR1
0.851 0.160 1 156913423 missense variant C/A;T snv 0.14; 4.0E-06 4
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs9295128 0.925 0.040 6 160330499 intergenic variant G/T snv 1.1E-02 2