Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2284411
GRIN2B
1.000 0.040 12 13713238 intron variant C/T snv 0.34 4
rs2110267
DPP6
1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 3
rs750257282
CARS1 ; CARS1-AS1
1.000 0.040 11 3038127 missense variant C/G;T snv 3.2E-05 3
rs875989839
PDE10A
1.000 6 165450242 missense variant C/G snv 3
rs1057519475
FOXC1
1.000 0.080 6 1610761 stop gained C/T snv 2
rs1170695
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11013652 5 prime UTR variant A/G snv 0.35 2
rs1331851285
CASP1
1.000 0.080 11 105029220 missense variant T/C snv 1.4E-05 2
rs1541665
KCNIP1
1.000 0.040 5 170715913 intron variant C/G;T snv 0.21 2
rs202247812
KRAS
1.000 0.160 12 25225717 missense variant T/C snv 2
rs2303380
TTC12
1.000 0.040 11 113329987 splice region variant G/A snv 0.61 0.64 2
rs2944366
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11011556 intron variant T/C snv 0.25 2
rs372857241
FOXC1
1.000 0.080 6 1610586 stop gained C/G;T snv 1.8E-05 2
rs6278
DRD2
1.000 0.080 11 113410002 3 prime UTR variant C/A snv 0.14 2
rs776423109
C3
1.000 0.120 19 6718117 missense variant G/A;T snv 4.0E-06; 4.0E-06 2
rs942758928
MC4R
1.000 0.080 18 60371854 missense variant C/T snv 8.0E-06 1.4E-05 2
rs9990174
SLC6A1
1.000 0.040 3 10998753 intron variant G/T snv 0.31 2
rs1057518644
HGSNAT
0.925 0.120 8 43192413 stop gained C/T snv 10
rs606231193
PQBP1
0.925 0.080 X 48902391 frameshift variant AGAG/-;AG;AGAGAG delins 6
rs778899140
PDE10A
0.925 6 165450268 missense variant T/C snv 4.0E-06 5
rs1800035
ADRA2A
0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs202151337
SCN8A
0.925 0.160 12 51806788 missense variant A/G snv 4
rs6191
NR3C1
0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4
rs121908672
LRP5
0.925 0.080 11 68357802 missense variant C/T snv 3
rs121918626
LOC102724058 ; SCN1A ; SCN1A-AS1
0.925 0.080 2 166012179 missense variant T/G snv 3
rs363043
SNAP25-AS1 ; SNAP25
0.925 0.080 20 10245498 intron variant C/T snv 0.30 3