Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs1441937959
EFL1
0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 20
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs1114167422
SNORA56 ; DKC1
0.776 0.320 X 154773148 missense variant A/G snv 11
rs771063992
DNAJC21
0.827 0.240 5 34937431 stop gained C/T snv 2.8E-05 2.8E-05 7
rs768849283
PRF1
0.882 0.040 10 70600517 missense variant C/G snv 6.8E-05 7
rs121918544
TINF2
0.827 0.200 14 24240635 missense variant C/T snv 7
rs1057520529
FOXP3
0.851 0.320 X 49251440 missense variant C/T snv 5
rs1555889984
RUNX1
0.925 0.120 21 34834536 stop gained C/A snv 5
rs28936072
DKC1
0.851 0.200 X 154765472 missense variant T/C snv 4
rs774568856
PGM3
0.882 0.200 6 83174481 missense variant A/G snv 1.7E-05 7.0E-06 4
rs1057517674
MAD2L2
0.925 0.040 1 11676926 missense variant A/T snv 2
rs878855337
SAMD9L
0.925 0.120 7 93132385 missense variant C/G snv 2
rs1374309197
TP53BP1
1.000 0.040 15 43492016 missense variant T/A;C snv 4.0E-06 7.0E-06 1