Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140511594
TTC21B ; TTC21B-AS1
0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs3764880
TLR8-AS1 ; TLR8
0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs315952
IL1RN
0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs11643718
SLC12A3
0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 10
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs37369
AGXT2
0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs4740
EBI3
0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs2276415
AQP11 ; CLNS1A
0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6