Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs10924303
LOC105373265 ; KIF26B
1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs12125049
LINC02778 ; LOC105378761
1.000 0.040 1 60202030 intergenic variant C/T snv 0.12 2
rs8079544
TP53
1.000 0.040 17 7676734 intron variant C/T snv 7.4E-02 2
rs8753
POLR2A
1.000 0.040 17 7514323 non coding transcript exon variant C/T snv 1.4E-02 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs1920116
LRRC31
0.882 0.040 3 169862183 intron variant G/A snv 0.25 5
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs63750790
MSH2
1.000 0.160 2 47476425 missense variant G/A snv 3.2E-05 7.0E-06 3
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs10924690
SMYD3
1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11166389
SLC35A3 ; RNU6-1318P
1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs11599775
VTI1A
1.000 0.040 10 112699938 intron variant G/A snv 0.27 2
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20 2
rs4252707
MDM4
1.000 0.040 1 204539019 intron variant G/A snv 0.17 2
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs1805389
LIG4
0.882 0.080 13 108211261 missense variant G/A;C;T snv 5.7E-02; 4.1E-06 4
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2