Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 2
rs16841143
PTH2R
2 208384849 intron variant G/A snv 0.13 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs1885884
HTR2A ; HTR2A-AS1
13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs228682
PER3
1 7796286 intron variant T/C snv 0.35 2
rs384005
MEF2C-AS2
5 88709286 intron variant T/C snv 0.70 2
rs4554696
PDE4B
1 65942328 intron variant C/T snv 0.33 2
rs571720664
DLG4
17 7203556 missense variant C/G;T snv 4.0E-06 2
rs62199592 2 183858773 intergenic variant A/G snv 2.1E-02 2
rs6475417
SLC24A2
9 20212043 intergenic variant A/G;T snv 2
rs6661750
PDE4B
1 66081201 intron variant A/G;T snv 2
rs9316235
HTR2A
13 46871568 intron variant G/A snv 0.19 2
rs10103191 8 91890204 intron variant G/A snv 0.58 1
rs1170191
DGKH
13 42101357 intron variant A/G;T snv 1
rs1382119307
CDSN ; PSORS1C1
6 31116450 missense variant C/G snv 7.0E-06 1
rs147634553
ITGA2B
17 44383518 synonymous variant G/A;T snv 6.5E-05; 4.1E-06 1
rs1653625
LOC105370032 ; P2RX7
12 121185082 3 prime UTR variant C/A;G snv 1
rs1657268
HTR5A
7 155082904 intron variant C/G;T snv 1
rs16940655
MAPT-AS1 ; LINC02210-CRHR1 ; CRHR1
17 45816520 missense variant C/A;T snv 4.0E-06; 6.4E-03 1
rs1801206
WFS1
4 6300980 stop gained C/G;T snv 0.63 1
rs1801213
WFS1
4 6291969 synonymous variant C/G snv 0.72 0.68 1
rs2167457
PC
11 66874925 intron variant C/T snv 0.25 1
rs2230739
ADCY9
16 3983435 missense variant T/A;C snv 4.4E-06; 0.29 1
rs2376803
LOC105378590
1 2036515 intergenic variant C/T snv 0.71 1