Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs1008805
MIR4713HG ; CYP19A1
0.851 0.160 15 51257402 intron variant G/A snv 0.64 7
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10473984
CRHBP
5 76971301 intron variant G/T snv 0.12 1
rs1080963 22 15376497 intergenic variant C/T snv 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10914456
HCRTR1
1.000 0.040 1 31622570 intron variant T/C snv 0.51 2
rs10997870
SIRT1
1.000 0.040 10 67908257 intron variant G/T snv 0.47 2
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs11046205
ABCC9
12 21839392 intron variant G/A snv 0.19 2
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs115482041
RCL1
0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs12137927
PER3
1 7811169 intron variant T/C snv 0.20 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1220000453
ZFP91-CNTF ; CNTF
0.882 0.120 11 58624189 synonymous variant C/T snv 5
rs12720208
FGF20
0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02 3
rs1290141855
SLC6A2
1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31