Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs1880481
CTNNB1
0.925 0.080 3 41230590 intron variant C/A snv 0.40 2
rs2243421
DAB2IP
0.925 0.080 9 121631045 intron variant C/T snv 0.44 2
rs11695471
DNMT3A
0.925 0.080 2 25234839 intron variant T/A;C snv 2
rs1801159
DPYD
0.925 0.080 1 97515839 missense variant T/C snv 0.20 0.18 2
rs2934971
ERBB2
0.925 0.080 17 39698254 intron variant G/T snv 0.66 2
rs2643194
ERBB2 ; PGAP3
0.925 0.080 17 39696795 5 prime UTR variant C/T snv 0.67 2
rs3202538
ERBB3 ; LOC105369782
0.925 0.080 12 56102447 3 prime UTR variant G/T snv 2
rs734004
EZH2
0.925 0.080 7 148808368 intron variant G/C snv 0.66 2