Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs779059411
PAX9
0.925 0.080 14 36666492 missense variant A/C;G snv 8.4E-06 2
rs121908568
AXIN2
0.807 0.160 17 65536495 stop gained G/A snv 9
rs758468472
NOL11 ; LOC101928045
0.776 0.160 17 67718094 splice region variant G/T snv 8
rs730882193
AXIN2
0.807 0.200 17 65536472 stop gained C/G;T snv 6
rs1567755946
AXIN2
0.925 0.080 17 65537563 frameshift variant -/CGCGGGAGGCAGC delins 2
rs752881223
AXIN2
0.925 0.080 17 65558307 missense variant A/C;G snv 2
rs1392844787
ZNF569
0.925 0.080 19 37413765 missense variant T/C;G snv 4.0E-06; 4.0E-06 2
rs1557036768
HUWE1
0.708 0.320 X 53647390 missense variant C/T snv 44
rs55846652 0.776 0.160 X 69564858 downstream gene variant T/C snv 0.29 8