Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10194776
PSMD1 ; HTR2B
2 231115305 intron variant C/T snv 0.54 1
rs10410239
CC2D1A
1.000 0.200 19 13919876 synonymous variant T/C snv 0.27 0.38 2
rs1047322213
PQBP1
1.000 0.120 X 48902470 missense variant G/A snv 2
rs104886492
HSD17B10
1.000 0.120 X 53432410 missense variant A/G snv 3
rs104894743
ARX
0.807 0.200 X 25012937 missense variant G/A snv 7
rs1052108705
TCF19 ; POU5F1
6 31165217 missense variant C/T snv 4.1E-06 2.1E-05 3
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 4
rs1131692042
RPL10 ; SNORA70
0.925 0.120 X 154399803 missense variant C/T snv 3
rs113994097
POLG
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs115466046
KCNJ10
1 160042480 missense variant C/T snv 1.2E-02 1.1E-02 2
rs1162306056
KCNQ3
0.882 0.080 8 132174294 missense variant C/T snv 5
rs1171889657
HADHB
2 26273656 missense variant T/C snv 4.0E-06 1
rs1177566365
RIMS2
8 103766303 missense variant G/T snv 4.0E-06 7.0E-06 1
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs121434612
PAK3
1.000 0.080 X 111142119 missense variant C/T snv 2
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 4
rs121434614
PAK3
0.925 0.200 X 111196570 missense variant G/C snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121917899
PQBP1
1.000 0.080 X 48901944 missense variant A/G snv 2
rs121918364
SRPX2
0.851 0.200 X 100662227 missense variant A/C snv 3.3E-05 2.9E-05 5
rs121918368
CRBN ; TRNT1
0.925 0.200 3 3150939 stop gained G/A snv 8.0E-06 7.0E-06 3
rs121918523
PHF8
0.925 0.200 X 54016662 stop gained T/A snv 3
rs121918524
PHF8
0.827 0.200 X 54011232 missense variant A/G snv 6
rs121918822
ASMT
Y 1642868 missense variant C/T snv 1