Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10230087
FOXP2
1.000 0.040 7 114614352 intron variant G/A snv 0.73 2
rs1023159
SLC19A1
1.000 0.040 21 45546266 intron variant G/A snv 0.34 1
rs1026306398
EN2
1.000 0.040 7 155458802 missense variant C/A;G;T snv 3.0E-04; 7.6E-05 1
rs1033810883
WNT10B ; WNT1
1.000 0.040 12 48979625 missense variant A/C snv 4.0E-06 1
rs10418707
DNMT1
1.000 0.040 19 10145541 intron variant G/A;T snv 0.11 1
rs10423341
DNMT1
1.000 0.040 19 10156590 intron variant C/A snv 0.13 1
rs1042778
CAV3 ; OXTR
0.925 0.040 3 8752859 3 prime UTR variant G/A;C;T snv 3
rs1049346
GLO1
0.882 0.080 6 38703061 5 prime UTR variant G/A snv 0.50 0.54 3
rs10497655
LOC105373780 ; ZNF804A
1.000 0.040 2 184597314 intron variant T/C;G snv 2
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs1060826
NOS2
0.851 0.160 17 27762841 synonymous variant T/C snv 0.66 0.67 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1085308043
PTEN
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs10951154
HOTAIRM1 ; HOXA1
0.925 0.040 7 27095695 missense variant C/A;G;T snv 0.76 2
rs11155819
ESR1
1.000 0.040 6 151878224 intron variant T/C snv 0.25 1
rs11236697
SHANK2
1.000 0.040 11 70576391 intron variant T/C snv 4.4E-02 1
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 13
rs1131692040
SNORA70 ; RPL10
0.882 0.160 X 154399844 missense variant A/G snv 4
rs1152582
ESR2 ; SYNE2
1.000 0.040 14 64225912 3 prime UTR variant G/A;C snv 1
rs1163276899
CACNA1D
1.000 0.040 3 53673125 missense variant G/A snv 2
rs11639084
RORA
0.851 0.200 15 60774317 intron variant C/T snv 0.20 4
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2