Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs733618
CTLA4
0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs75002266
ORC4
0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs149207840
SP140
0.851 0.160 2 230279864 intron variant CTGCCTC/-;CTGCCTCCTGCCTC delins 0.15 4
rs6546149
DTNB
0.851 0.160 2 25406569 intron variant C/G snv 0.38 4
rs756168629
LRP1B
1.000 0.160 2 140841050 missense variant C/T snv 4.8E-05 1.4E-05 2
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 2
rs1006752
DTNB-AS1 ; DTNB
1.000 0.160 2 25441122 intron variant C/T snv 0.12 1
rs10180663
DTNB
1.000 0.160 2 25410373 intron variant T/A;C;G snv 1
rs1250801605
CASP10
1.000 0.160 2 201185809 missense variant G/A snv 4.0E-06 1
rs13387987
DTNB
1.000 0.160 2 25459547 intron variant G/A snv 0.29 1
rs13390436
DTNB
1.000 0.160 2 25447908 intron variant C/T snv 0.28 1
rs13397493
DTNB
1.000 0.160 2 25449823 intron variant C/T snv 0.24 1
rs2036653
DTNB
1.000 0.160 2 25444100 intron variant A/T snv 0.28 1
rs2384232
DTNB
1.000 0.160 2 25400880 intron variant G/A snv 0.38 1
rs28801070 1.000 0.160 2 185380090 intergenic variant G/A snv 1
rs4325816
SP3
1.000 0.160 2 173944171 intron variant T/C snv 0.20 1
rs55924491
DTNB
1.000 0.160 2 25382154 intron variant C/G snv 0.13 1
rs559979934
CASP10
1.000 0.160 2 201185838 missense variant C/G;T snv 4.8E-05 2.1E-05 1
rs61070260
LRP1B
1.000 0.160 2 140846426 intron variant G/A snv 5.7E-02 1
rs6546183
DTNB
1.000 0.160 2 25448937 intron variant G/A;T snv 1
rs6546184
DTNB
1.000 0.160 2 25449600 intron variant C/T snv 0.26 1
rs6746082
DTNB ; DTNB-AS1
1.000 0.160 2 25436375 intron variant A/C;T snv 1
rs6761076
DTNB
1.000 0.160 2 25384889 intron variant T/C snv 0.25 1