Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs746800707
AAR2
0.851 0.160 20 36240388 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 8
rs72664233
ABCC6
0.882 0.200 16 16157770 frameshift variant A/- del 8.4E-05 4.9E-05 10
rs63750427
ABCC6
0.882 0.200 16 16163158 missense variant C/G;T snv 4.0E-06; 1.2E-05 6
rs1285524167
ABCC8
0.807 0.280 11 17475004 missense variant C/T snv 8.0E-06 8
rs864309499
ACO2 ; POLR3H
0.827 0.240 22 41526319 missense variant C/T snv 4.0E-06 9
rs1131692228
ACTL6B
0.925 0.160 7 100646637 missense variant C/T snv 5
rs1060499738
ACTL6B
1.000 7 100647014 missense variant C/T snv 7.0E-06 2
rs1562846694
ACTL6B ; TFR2
0.763 0.320 7 100643252 inframe deletion TTCGCTCCACGCACT/- delins 32
rs587776625
ADGRG1
0.851 0.080 16 57654103 frameshift variant CAGGACC/- delins 12
rs1567815105
ADGRG1
0.807 0.240 16 57660794 frameshift variant -/T delins 7
rs1057518345
ADNP
0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs886041116
ADNP
0.776 0.240 20 50892526 stop gained G/A snv 13
rs1131692272
AFF3
0.851 0.240 2 100006808 missense variant C/T snv 9
rs1564069807
AGTPBP1
0.925 0.040 9 85619213 splice donor variant A/C snv 3
rs1564069651
AGTPBP1
1.000 9 85619123 missense variant T/C snv 2
rs587779766
AHDC1
0.851 0.200 1 27549742 frameshift variant CA/- delins 7
rs587779767
AHDC1
0.851 0.200 1 27549218 frameshift variant G/- delins 7
rs587779768
AHDC1
0.851 0.200 1 27549569 frameshift variant G/- delins 7
rs121434350
AHI1
0.882 0.240 6 135455750 missense variant A/T snv 3
rs587776935
AKT3
0.827 0.120 1 243505296 missense variant G/A snv 7
rs863225045
ALDH18A1
0.790 0.360 10 95637327 missense variant C/A;T snv 15
rs398122394
ALG13
0.763 0.240 X 111685040 missense variant A/G snv 17
rs1569508922
ALG13
0.882 0.160 X 111681268 missense variant T/A snv 5
rs1560162116
ALG3
0.882 0.080 3 184242930 missense variant T/C snv 5
rs1560164682
ALG3
0.882 0.080 3 184245709 splice region variant T/C snv 5