Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
rs7529229
IL6R
0.851 0.120 1 154448302 intron variant T/C snv 0.48 8
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 7
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs1044925
SOAT1
0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 6
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs5938
PTAFR
0.827 0.200 1 28150351 missense variant G/T snv 8.0E-03 2.5E-03 5
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs313152
PTAFR
0.851 0.120 1 28149490 3 prime UTR variant T/C snv 0.29 4
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4
rs6131
SELP
0.851 0.200 1 169611647 missense variant C/T snv 0.20 0.22 4
rs762079672
AGT
0.882 0.040 1 230710211 missense variant C/T snv 4.0E-06 4
rs10159239
NLRP3
0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs10918859
NOS1AP
0.882 0.040 1 162199478 intron variant G/A snv 0.16 3