Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 1
rs1982350
ARNTL
11 13328584 intron variant A/G snv 0.57 1
rs267606826
FOXG1
0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 28
rs1448259271
IRF2BPL ; LOC107984638
0.790 0.240 14 77027279 stop gained C/A;T snv 23
rs555145190
NAGLU
0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs1564421528
WAC
0.882 0.080 10 28614666 stop gained C/T snv 16
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 8
rs1555358382
GCH1
14 54844115 stop gained G/A snv 6
rs773685207
MED13
0.851 0.200 17 61966645 stop gained G/A;C;T snv 4.3E-06; 4.3E-05 6
rs1057521223
SCN2A
1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs1557043622
SLC35A2
0.695 0.400 X 48909843 missense variant C/A snv 46
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 40
rs1057524820
SCN8A
0.776 0.280 12 51765746 missense variant G/A;T snv 33
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs148881970
NAGLU
0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs1085307845
PHIP
0.752 0.320 6 79025582 missense variant G/T snv 21
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs1057524157
DEAF1
0.776 0.200 11 686962 missense variant A/C;T snv 19
rs529855742
SGSH
0.827 0.320 17 80214291 missense variant G/A snv 1.2E-05 1.4E-05 15
rs1554944271
DEAF1
0.851 0.240 11 686925 missense variant C/G snv 14