Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs17568
TNFRSF4
0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 7
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 7
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs2070150
ATF6
0.827 0.280 1 161791486 missense variant G/C snv 0.14 9.2E-02 6
rs4641
LMNA
0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs150924946
LMNA
0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs2275558
PBX1
0.882 0.200 1 164559883 missense variant G/A snv 0.30 0.19 5
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs60662302
LMNA
0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs7212
TXNIP
0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5