Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1290141855
SLC6A2
1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 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
rs161645
LOC105379109
1.000 0.040 5 104734216 intron variant A/G snv 0.77 2
rs228644
PER3
1.000 0.080 1 7806023 intron variant G/A snv 0.36 2
rs3821831
ITIH4
1.000 0.040 3 52819385 splice region variant C/T snv 0.29 0.29 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
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs115482041
RCL1
0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs1876831
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 4
rs6191
NR3C1
0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 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
rs2228305
FASN
0.925 0.120 17 82084916 missense variant C/T snv 4.1E-02 4.5E-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
rs9536314
KL
0.925 0.160 13 33054001 missense variant T/A;G snv 0.14 3
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs1220000453
ZFP91-CNTF ; CNTF
0.882 0.120 11 58624189 synonymous variant C/T snv 5
rs680244
CHRNA5
0.882 0.120 15 78578946 intron variant T/C snv 0.60 4
rs757891309
MTR
0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06 4