Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs767181086
LAMC2
0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs10864315
PER3
1 7790021 intron variant C/T snv 0.28 3
rs1057521223
SCN2A
1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs1060499733
DHX30
0.851 0.120 3 47846757 missense variant A/G snv 11
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs146539065
SEPSECS
0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714
SEPSECS
0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1380822792
NAA15
0.882 0.080 4 139336933 frameshift variant CTTGA/- delins 7
rs3805148
TMEM165 ; CLOCK
4 55440643 intron variant A/C snv 0.33 3
rs1131692231
CYFIP2
0.827 0.280 5 157294834 missense variant C/T snv 13
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1085307845
PHIP
0.752 0.320 6 79025582 missense variant G/T snv 21
rs1562114190
IRAK1BP1 ; PHIP
0.790 0.160 6 78946061 frameshift variant A/- delins 21
rs1562171209
PHIP
0.851 0.160 6 79003821 missense variant T/C snv 9
rs755246809
AHI1
0.827 0.280 6 135404951 frameshift variant T/- delins 5.9E-04 4.9E-05 7
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs1554317002
LOC112267983 ; CDK13
0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs142110773
FIGNL1 ; DDC
0.882 0.160 7 50463317 missense variant G/A snv 1.6E-05 7.0E-06 13
rs4719714
STEAP1B
1.000 0.080 7 22721094 intron variant A/T snv 0.21 5