Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1784692
ZBTB16
1.000 0.120 11 114078510 intron variant T/C snv 0.17 1
rs11225138
YAP1
0.925 0.200 11 102123167 intron variant G/C snv 6.1E-02 2
rs11225154
YAP1
1.000 0.120 11 102172509 intron variant G/A;C snv 1
rs11225161
YAP1
1.000 0.120 11 102199763 intron variant C/T snv 7.0E-02 1
rs1894116
YAP1
1.000 0.120 11 102199908 intron variant A/G snv 8.2E-02 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs3025020
VEGFA
0.882 0.240 6 43781373 non coding transcript exon variant C/T snv 0.24 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs757343
VDR
0.807 0.360 12 47845892 intron variant C/T snv 0.12 6
rs10514258
VCAN-AS1 ; VCAN
1.000 0.120 5 83575938 intron variant A/G snv 0.13 1
rs17008097
USP34
1.000 0.120 2 61295935 intron variant C/G snv 0.15 1
rs17008940
USP34
1.000 0.120 2 61391463 intron variant C/T snv 0.12 1
rs3756159
UBA6-AS1 ; GNRHR
0.882 0.160 4 67756760 intron variant G/A snv 0.44 3
rs12644822
UBA6-AS1 ; GNRHR
1.000 0.120 4 67756817 intron variant G/A snv 0.33 1
rs13138607
UBA6-AS1 ; GNRHR
1.000 0.120 4 67755832 intron variant G/A snv 0.44 1
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169