Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7768897
AMD1
0.925 0.080 6 110891080 non coding transcript exon variant A/G;T snv 2
rs1400295986
APC
0.925 0.080 5 112838233 missense variant T/C snv 2
rs28933379
APC
1.000 0.080 5 112838953 missense variant G/A snv 2
rs2279284
ARNTL
0.925 0.080 11 13277203 intron variant C/T snv 0.25 2
rs911160
AURKA
0.925 0.080 20 56382507 intron variant G/A;C snv 2
rs2241909
AURKB
0.925 0.080 17 8205021 synonymous variant G/A snv 0.66 0.64 2
rs2289590
AURKB
0.925 0.080 17 8207446 intron variant C/A snv 0.54 2
rs11084490
AURKC
0.925 0.080 19 57231104 5 prime UTR variant G/A;C;T snv 0.87; 3.8E-05 2
rs758099
AURKC
0.925 0.080 19 57231966 intron variant C/G;T snv 2
rs1044432
BTBD10
0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 2
rs384490
CARS1
0.925 0.080 11 3057655 splice region variant T/G snv 0.46 2
rs729662
CARS1
0.925 0.080 11 3006910 synonymous variant G/A snv 0.35 0.25 2
rs7394702
CARS1
0.925 0.080 11 3022918 intron variant T/C snv 0.17 2
rs121909776
CASP10
1.000 0.080 2 201187798 missense variant T/C snv 1.2E-04 2.8E-05 2
rs4647693
CASP3
0.925 0.080 4 184629610 intron variant T/C snv 0.31 2
rs10787498
CASP7
0.925 0.080 10 113729891 3 prime UTR variant T/G snv 0.38 2
rs1127687
CASP7
0.925 0.080 10 113730350 3 prime UTR variant G/A snv 0.23 2
rs12247479
CASP7
0.925 0.080 10 113730301 3 prime UTR variant G/A snv 0.16 2
rs746782366
CBS
0.925 0.120 21 43072117 missense variant C/G;T snv 8.1E-06; 4.0E-06 2
rs77447679
CBX4
0.925 0.080 17 79836675 intron variant C/A snv 5.4E-02 2
rs17690554
CDH1
0.925 0.080 16 68835607 downstream gene variant C/G;T snv 2
rs11133399
CLOCK
0.925 0.080 4 55547664 non coding transcript exon variant A/G snv 0.28 2
rs11170877
COPZ1
0.925 0.080 12 54340505 start lost A/G snv 0.16 0.17 2
rs12231393
COPZ1
0.925 0.080 12 54318989 intron variant T/C snv 0.14 2
rs7208768
CRK
0.925 0.080 17 1449407 intron variant G/A snv 0.56 2