Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs1057520063
GLI3
0.763 0.200 7 41964641 frameshift variant -/A delins 13
rs398123425
ATRX
0.776 0.320 X 77688876 missense variant T/C snv 9
rs568887534
DCTN6
0.807 0.240 8 30183156 missense variant A/G snv 4.0E-06 9
rs1250394819
LOC101927100 ; TMED7-TICAM2 ; TMED7
0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06 9
rs1190999960
ZNRD2-AS1 ; ZNRD2 ; FAM89B
0.807 0.240 11 65571690 missense variant G/A snv 9
rs886039811
B9D1
0.807 0.320 17 19357875 missense variant A/G snv 4.0E-06 6
rs148634289
SDHD
0.827 0.200 11 112088925 synonymous variant C/T snv 1.6E-05 2.1E-05 6
rs1285675735
SORD
0.827 0.200 15 45043384 synonymous variant C/G;T snv 1.1E-05; 1.1E-05 6
rs587780072
TP53
0.882 0.240 17 7674927 missense variant G/A;C snv 2.8E-05 3
rs11893842
OBSL1 ; INHA
0.925 0.160 2 219572251 intron variant A/G snv 0.45 2
rs1464311 1.000 0.080 3 118482382 intron variant T/C snv 0.12 1
rs587777706
BMS1
1.000 0.080 10 42820527 missense variant G/A snv 1.6E-05 1.4E-05 1