Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs164147
rs164147
NOS1AP
3 0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 0.010 1.000 1 2016 2016
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs1800797
rs1800797
IL6 ; STEAP1B ; IL6-AS1
43 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 0.010 1.000 1 2010 2010
dbSNP: rs1801260
rs1801260
CLOCK ; TMEM165
28 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 0.010 1.000 1 2019 2019
dbSNP: rs193922262
rs193922262
GCK
2 0.925 0.080 7 44145636 stop gained C/A;G snv 4.3E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs193922287
rs193922287
GCK
2 0.925 0.080 7 44153334 missense variant G/A snv 4.0E-06 0.010 < 0.001 1 2013 2013
dbSNP: rs193922289
rs193922289
GCK
3 0.882 0.080 7 44152420 missense variant C/T snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs193929375
rs193929375
GCK
3 0.882 0.120 7 44145560 missense variant C/A snv 0.010 1.000 1 2005 2005
dbSNP: rs2241766
rs2241766
ADIPOQ ; ADIPOQ-AS1
48 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 0.010 1.000 1 2006 2006
dbSNP: rs2273773
rs2273773
SIRT1
9 0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs2282018
rs2282018
AVP
1 1.000 0.040 20 3084303 intron variant C/T snv 0.60 0.010 1.000 1 2016 2016
dbSNP: rs2770381
rs2770381 		1 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 0.010 1.000 1 2016 2016
dbSNP: rs290487
rs290487
TCF7L2
10 0.776 0.280 10 113149972 intron variant C/T snv 0.16 0.010 1.000 1 2020 2020
dbSNP: rs340874
rs340874
PROX1 ; PROX1-AS1
7 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 0.010 1.000 1 2014 2014
dbSNP: rs373269573
rs373269573
EHMT1
2 0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 0.010 < 0.001 1 2002 2002
dbSNP: rs3738435
rs3738435
CHRM3
2 0.925 0.080 1 239907303 intron variant T/C snv 0.23 0.010 < 0.001 1 2011 2011
dbSNP: rs3856806
rs3856806
PPARG
41 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2018 2018
dbSNP: rs397514580
rs397514580
GCK ; LOC105375258
2 0.925 0.080 7 44146467 missense variant C/T snv 0.010 1.000 1 2011 2011
dbSNP: rs4402960
rs4402960
IGF2BP2
21 0.724 0.400 3 185793899 intron variant G/T snv 0.38 0.010 1.000 1 2008 2008
dbSNP: rs4436578
rs4436578
DRD2
4 0.925 0.080 11 113436043 intron variant C/T snv 0.73 0.010 1.000 1 2019 2019
dbSNP: rs4580704
rs4580704
CLOCK
13 0.790 0.200 4 55460540 intron variant G/C snv 0.69 0.010 1.000 1 2019 2019
dbSNP: rs4644
rs4644
LGALS3
14 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 0.010 1.000 1 2016 2016
dbSNP: rs4994
rs4994
ADRB3
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.010 1.000 1 2018 2018
dbSNP: rs518147
rs518147
HTR2C
7 0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs534828104
rs534828104
AHSG
2 0.925 0.080 3 186618566 missense variant A/G snv 0.010 1.000 1 2018 2018