Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777042
CYC1
0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs572115942
PHKG2
0.925 0.240 16 30756714 missense variant G/A snv 8.0E-05 7.7E-05 7
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs561017686
NEUROD1 ; CERKL
0.882 0.120 2 181678138 missense variant G/A;C snv 8.0E-06; 8.4E-04 4
rs556581174
GCK
0.925 0.080 7 44145637 stop gained G/A;C;T snv 2
rs534828104
AHSG
0.925 0.080 3 186618566 missense variant A/G snv 2
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs397514580
GCK ; LOC105375258
0.925 0.080 7 44146467 missense variant C/T snv 2
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs3738435
CHRM3
0.925 0.080 1 239907303 intron variant T/C snv 0.23 2
rs373269573
EHMT1
0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 2
rs369841551
MC4R
0.882 0.120 18 60371884 stop gained G/A;T snv 4.0E-06 3
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs2770381 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 1
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs193929375
GCK
0.882 0.120 7 44145560 missense variant C/A snv 3