Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6610650 1.000 0.040 X 37777261 intron variant G/A snv 0.27 2
rs869025495
NPHS2
0.851 0.080 1 179564715 missense variant G/A snv 6
rs3923647
TLR1
0.925 0.080 4 38797918 missense variant T/A;C;G snv 2.7E-02; 4.0E-06; 1.6E-05 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs11122576
AGT
1.000 0.080 1 230710933 intron variant T/C snv 8.2E-02 2
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs1926723
AGT
1.000 0.080 1 230704350 intron variant T/A;C;G snv 1.2E-05; 0.11; 2.0E-05 2
rs3729548
SLC2A1
1.000 0.080 1 42934681 intron variant C/T snv 0.32 2
rs7704116
PPP2CA
1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 2
rs37369
AGXT2
0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs2607420
ITPKC
0.925 0.120 19 40738982 intron variant G/A snv 0.76 3
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs1888747
FRMD3
1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs3115573 1.000 0.120 6 32251066 upstream gene variant A/G snv 0.41 2
rs9357155
PSMB8
1.000 0.120 6 32842071 non coding transcript exon variant G/A;C snv 2
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs2228226
GLI1 ; ARHGAP9
0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6
rs2276415
AQP11 ; CLNS1A
0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6