Disease: Agenesis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs4904210
PAX9
0.851 0.080 14 36666548 missense variant G/C snv 0.36 0.33 5
rs8670
MSX1
0.925 0.080 4 4863149 3 prime UTR variant C/T snv 0.22 0.23 4
rs929387
GLI3
0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs1095
MSX1
0.925 0.080 4 4863211 3 prime UTR variant C/T snv 1.5E-02 2
rs11001553
PRKG1-AS1 ; DKK1
0.925 0.080 10 52313141 intron variant C/T snv 0.12 2