Disease: Sleep Disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11600996
ARNTL
1.000 0.040 11 13374619 intron variant T/C snv 0.40 4
rs35275025
PER1
1.000 0.080 17 8141219 missense variant C/G;T snv 4.0E-06 3
rs4719714
STEAP1B
1.000 0.080 7 22721094 intron variant A/T snv 0.21 5
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs1229030855
TIMELESS
0.925 0.080 12 56428321 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs2291739
TIMELESS
0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs3789327
ARNTL
0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs9315202 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 4
rs9563121
KL
0.925 0.080 13 33050369 intron variant C/T snv 0.26 4
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs767181086
LAMC2
0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 14
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59