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: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.060 0.833 6 2012 2019
dbSNP: rs17782313
rs17782313 		34 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 0.040 1.000 4 2010 2018
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.030 1.000 3 2009 2018
dbSNP: rs1137101
rs1137101
LEPR
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2018 2018
dbSNP: rs1232898090
rs1232898090
PPARA
40 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 0.020 1.000 2 2005 2006
dbSNP: rs149106723
rs149106723
NMU
1 1.000 0.080 4 55599178 missense variant G/A snv 1.6E-05 4.2E-05 0.020 1.000 2 2006 2009
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.020 1.000 2 2009 2016
dbSNP: rs4994
rs4994
ADRB3
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.020 1.000 2 2000 2015
dbSNP: rs6232
rs6232
PCSK1 ; LOC101929710
2 0.925 0.080 5 96416081 missense variant T/C snv 3.9E-02 3.2E-02 0.020 1.000 2 2014 2017
dbSNP: rs7895833
rs7895833 		12 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.020 1.000 2 2015 2016
dbSNP: rs1010553
rs1010553
STAB1
2 1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 0.010 1.000 1 2019 2019
dbSNP: rs12500837
rs12500837
NMU
1 1.000 0.080 4 55627872 intron variant T/C snv 0.21 0.010 1.000 1 2017 2017
dbSNP: rs1256046734
rs1256046734
LEPR
12 0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1319501
rs1319501
NAMPT
4 0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 0.010 1.000 1 2015 2015
dbSNP: rs1416580204
rs1416580204
MOK
49 0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.010 < 0.001 1 2014 2014
dbSNP: rs1501299
rs1501299
ADIPOQ ; ADIPOQ-AS1
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.010 1.000 1 2017 2017
dbSNP: rs162430
rs162430
PYY
1 1.000 0.080 17 43953041 3 prime UTR variant G/A snv 0.23 0.010 1.000 1 2007 2007
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.010 < 0.001 1 2014 2014
dbSNP: rs1800437
rs1800437
GIPR
13 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 0.010 1.000 1 2010 2010
dbSNP: rs1800849
rs1800849
UCP3
5 0.851 0.160 11 74009120 upstream gene variant G/A;T snv 0.010 1.000 1 2007 2007
dbSNP: rs1996023
rs1996023 		3 0.925 0.120 4 45162620 intergenic variant T/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs2016266
rs2016266
SP7
3 1.000 0.080 12 53334171 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs2030323
rs2030323
BDNF
6 0.925 0.080 11 27706992 intron variant A/C snv 0.83 0.010 1.000 1 2017 2017