Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10157763
AKT3
1.000 0.040 1 243831739 intron variant T/A;C snv 2
rs10496964 0.925 0.040 2 144602342 intergenic variant C/T snv 0.12 2
rs11663316 1.000 0.040 18 9027916 intergenic variant T/A snv 0.34 2
rs1178326
HDAC9
1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02 2
rs118166657 1.000 0.040 14 63580544 intergenic variant C/G snv 1.3E-02 2
rs12059546
CHRM3
0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs121918321
STXBP1
0.925 0.040 9 127675855 stop gained C/T snv 2
rs12668095
LOC105375268
1.000 0.040 7 47036178 intron variant G/A;C snv 2
rs13287547
C9orf92
1.000 0.040 9 16286892 intron variant A/G snv 0.32 2
rs139427007
LOC105369927 ; LOC105369928
1.000 0.040 12 97202325 intergenic variant A/T snv 6.3E-05 2
rs141860749
SYT2
1.000 0.040 1 202668176 intron variant C/A snv 2.7E-04 2
rs1429264
COTL1
1.000 0.040 16 84589878 intron variant T/C snv 0.28 2
rs143543475 1.000 0.040 10 27419100 upstream gene variant G/C snv 8.0E-02 2
rs144133667
LIAS
0.925 0.040 4 39470027 missense variant G/A snv 4.0E-06 7.0E-06 2
rs146173241 1.000 0.040 10 116285226 downstream gene variant C/T snv 7.1E-03 2
rs148173957
LOC105378976
1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 2
rs149055334
EFHC1
0.925 0.040 6 52424111 missense variant C/A snv 1.9E-03 7.7E-03 2
rs150435906
LOC107986950
1.000 0.040 8 65952103 intergenic variant G/T snv 2.7E-04 2
rs1553709855
ATP6V1A
0.925 0.040 3 113784310 missense variant G/T snv 2
rs1553710664
ATP6V1A
0.925 0.040 3 113794928 missense variant G/A snv 2
rs17084405 1.000 0.040 18 71429162 intergenic variant G/A snv 0.13 2
rs199542988
FOXRED1
1.000 0.040 11 126277489 missense variant G/A;T snv 1.2E-05; 4.0E-06 2
rs2279020
GABRA1
1.000 0.040 5 161895883 non coding transcript exon variant G/A snv 0.62 0.63 2
rs2292096
CAMSAP2
0.925 0.040 1 200857641 3 prime UTR variant A/G snv 0.14 2
rs2304016
SCN2A
0.925 0.040 2 165311993 intron variant A/G snv 1.2E-02 4.8E-03 2