Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6191
NR3C1
0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4
rs680244
CHRNA5
0.882 0.120 15 78578946 intron variant T/C snv 0.60 4
rs948854
GAL ; LOC107984343
0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65 4
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs12720208
FGF20
0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02 3
rs80356773
GBA
0.925 0.080 1 155235002 missense variant C/T snv 3
rs936306
MIR4713HG ; CYP19A1
0.925 0.080 15 51287401 intron variant C/T snv 0.30 3
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
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
rs11046205
ABCC9
12 21839392 intron variant G/A snv 0.19 2
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs161645
LOC105379109
1.000 0.040 5 104734216 intron variant A/G snv 0.77 2
rs17689882
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
17 45829462 intron variant G/A snv 0.14 2
rs2175898
ESR1
6 151875817 intron variant C/G;T snv 2
rs228644
PER3
1.000 0.080 1 7806023 intron variant G/A snv 0.36 2
rs228682
PER3
1 7796286 intron variant T/C snv 0.35 2
rs7208505
SKA2
1.000 0.040 17 59110368 3 prime UTR variant G/A;C;T snv 2
rs736408
ITIH3
1.000 0.040 3 52801338 intron variant C/T snv 0.47 2
rs10473984
CRHBP
5 76971301 intron variant G/T snv 0.12 1
rs1080963 22 15376497 intergenic variant C/T snv 1
rs12137927
PER3
1 7811169 intron variant T/C snv 0.20 1
rs138191010 7 145416641 intergenic variant G/T snv 1
rs1475157 6 6016936 intergenic variant A/G snv 0.17 1
rs2965087
LOC101927870 ; RELN
7 103471538 intron variant T/C snv 0.45 1