Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs11994014 0.827 0.200 8 24944767 intergenic variant A/G snv 0.70 5
rs201216664
NME1-NME2 ; NME2
0.851 0.080 17 51171503 missense variant A/G snv 5
rs74315406
PRNP
0.851 0.160 20 4699870 missense variant A/G snv 5
rs10895322
MMP20
0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 4
rs6939340
CASC15 ; NBAT1
0.851 0.160 6 22139775 intron variant A/G snv 0.62 4
rs10055201
IL31RA
0.882 0.080 5 55865274 intron variant A/G snv 0.76 3
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs17489363
SNHG31 ; BARD1
0.882 0.080 2 214809617 5 prime UTR variant A/G snv 0.73 0.74 3
rs3768707
BARD1
0.882 0.080 2 214780411 intron variant A/G snv 0.74 3
rs7973450
KRAS
0.882 0.080 12 25208208 3 prime UTR variant A/G snv 0.20 3
rs201698323
SCN10A
0.851 0.120 3 38742448 missense variant A/G;T snv 5.9E-04 4
rs758576072
RIMS2
0.851 0.160 8 104244917 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs121909536
ANG ; RNASE4
0.827 0.120 14 20693686 missense variant A/T snv 1.2E-03 9.4E-04 5
rs1211164799
DLX4
0.882 0.080 17 49973938 missense variant A/T snv 3
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2168101
LMO1 ; LOC105376536
0.827 0.200 11 8233861 intron variant C/A snv 0.24 7
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs104893855
PHOX2B-AS1 ; PHOX2B
0.851 0.160 4 41747479 missense variant C/A snv 4
rs143864187
CASP4
0.882 0.080 11 104949666 missense variant C/A snv 3
rs2302616
ODC1-DT ; ODC1 ; SNORA80B
0.882 0.080 2 10448065 intron variant C/A snv 0.26 3
rs75183227
TH
0.882 0.080 11 2169790 missense variant C/A snv 3
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58 3