Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886040971
TRPS1
0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs1057518972
TRPS1
0.827 0.200 8 115418359 missense variant C/T snv 7
rs368166434
TRPS1
0.851 0.200 8 115603883 stop gained G/A;C snv 4
rs121908435
TRPS1
0.925 0.160 8 115418391 missense variant C/G;T snv 2
rs121908436
TRPS1
0.925 0.160 8 115418358 missense variant G/A snv 2
rs1554593085
TRPS1
0.925 0.160 8 115587497 frameshift variant GATGTCCTGT/- delins 2
rs1554596063
TRPS1
0.925 0.160 8 115604319 frameshift variant GC/- del 2
rs1563623987
TRPS1
0.925 0.160 8 115587133 stop gained A/C snv 2
rs1563637033
TRPS1
0.925 0.160 8 115604264 frameshift variant ATGGAGCTGTT/- delins 2
rs1563638577
TRPS1
0.925 0.160 8 115604951 frameshift variant -/GCAA delins 2
rs28939069
TRPS1
0.925 0.160 8 115415015 missense variant G/A snv 2
rs28939070
TRPS1
0.925 0.160 8 115415014 missense variant C/T snv 2
rs751565386
TRPS1
0.925 0.160 8 115418392 stop gained G/A;T snv 8.0E-06 2
rs121908430
TRPS1
1.000 0.080 8 115604916 stop gained G/T snv 1
rs121908431
TRPS1
1.000 0.080 8 115604099 stop gained G/A;C snv 8.0E-06 1
rs121908432
TRPS1
1.000 0.080 8 115587144 stop gained G/A snv 1
rs121908434
TRPS1
1.000 0.080 8 115414593 stop gained G/C snv 1
rs1554592981
TRPS1
1.000 0.080 8 115587306 frameshift variant -/G delins 1
rs1554592995
TRPS1
1.000 0.080 8 115587345 frameshift variant CT/- delins 1
rs1554593099
TRPS1
1.000 0.080 8 115587521 frameshift variant CA/- delins 1
rs1554595857
TRPS1
1.000 0.080 8 115603875 stop gained G/T snv 1
rs1554595930
TRPS1
1.000 0.080 8 115604087 stop gained G/A snv 1
rs1554596193
TRPS1
1.000 0.080 8 115604509 frameshift variant T/- delins 1
rs1554596300
TRPS1
1.000 0.080 8 115604737 frameshift variant -/G delins 1
rs1554596328
TRPS1
1.000 0.080 8 115604792 frameshift variant -/A delins 1