Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs1805389
LIG4
0.882 0.080 13 108211261 missense variant G/A;C;T snv 5.7E-02; 4.1E-06 4
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
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
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs10924303
LOC105373265 ; KIF26B
1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690
SMYD3
1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs11166389
SLC35A3 ; RNU6-1318P
1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs111696067
GOLGA3
1.000 0.040 12 132799954 intron variant T/C snv 5.3E-04 2
rs11583706
LOC105373220
1.000 0.040 1 238358337 intron variant G/T snv 0.17 2
rs11598018
STN1
1.000 0.040 10 103901557 intron variant C/A;T snv 2