Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3805148
TMEM165 ; CLOCK
4 55440643 intron variant A/C snv 0.33 3
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs3789327
ARNTL
0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs1982350
ARNTL
11 13328584 intron variant A/G snv 0.57 4
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1229030855
TIMELESS
0.925 0.080 12 56428321 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs4719714
STEAP1B
1.000 0.080 7 22721094 intron variant A/T snv 0.21 5
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs35275025
PER1
1.000 0.080 17 8141219 missense variant C/G;T snv 4.0E-06 3
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 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
rs10864315
PER3
1 7790021 intron variant C/T snv 0.28 3
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25