Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs11202592
KLLN ; PTEN
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs9906827
RPTOR
0.925 0.120 17 80691605 intron variant C/A;T snv 2
rs10515074
PIK3R1
0.925 0.120 5 68270365 intron variant A/G;T snv 2
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs146488435
KCNH6
0.851 0.080 17 63533914 missense variant C/G;T snv 8.0E-06; 6.4E-05 5
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs369841551
MC4R
0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 3
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs750931344
SLC38A4
1.000 0.040 12 46769424 missense variant C/T snv 4.0E-06 1
rs1018185646
HNF4A
1.000 0.040 20 44428455 missense variant T/C snv 4.0E-06 1
rs1375557127
HNF4A
0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 2
rs1392795567
HNF4A
0.925 0.080 20 44414663 splice donor variant G/A snv 2
rs1568724014
MIR3646 ; HNF4A
0.925 0.080 20 44407421 stop gained C/T snv 2
rs1385251852
MIR3646 ; HNF4A
0.925 0.080 20 44406208 frameshift variant G/- delins 2