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: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.040 0.750 4 2006 2017
dbSNP: rs12255372
rs12255372
TCF7L2
28 0.667 0.480 10 113049143 intron variant G/A;T snv 0.030 1.000 3 2006 2011
dbSNP: rs4402960
rs4402960
IGF2BP2
21 0.724 0.400 3 185793899 intron variant G/T snv 0.38 0.020 1.000 2 2010 2014
dbSNP: rs560887
rs560887
SPC25 ; G6PC2
18 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.020 1.000 2 2009 2010
dbSNP: rs10830963
rs10830963
MTNR1B
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.010 1.000 1 2009 2009
dbSNP: rs11061946
rs11061946
ADIPOR2
2 1.000 0.080 12 1719361 intron variant C/T snv 6.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs11061973
rs11061973
ADIPOR2
2 1.000 0.080 12 1756770 intron variant G/A snv 0.12 0.010 1.000 1 2011 2011
dbSNP: rs11136000
rs11136000
CLU
19 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.010 1.000 1 2017 2017
dbSNP: rs1527483
rs1527483
CD36
2 1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs17446593
rs17446593 		2 1.000 0.080 13 40553948 intron variant A/G snv 0.19 0.010 1.000 1 2009 2009
dbSNP: rs17446614
rs17446614
FOXO1
5 0.851 0.240 13 40565740 intron variant G/A snv 0.16 0.010 1.000 1 2009 2009
dbSNP: rs2297627
rs2297627
FOXO1
3 0.925 0.120 13 40659794 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
dbSNP: rs2721068
rs2721068
FOXO1
4 0.882 0.160 13 40565575 intron variant T/C snv 0.38 0.010 1.000 1 2009 2009
dbSNP: rs2920502
rs2920502
PPARG
6 0.851 0.160 3 12287696 intron variant G/C snv 0.27 0.010 1.000 1 2018 2018
dbSNP: rs3731201
rs3731201
CDKN2A
2 1.000 0.080 9 21988897 intron variant C/T snv 0.86 0.010 1.000 1 2010 2010
dbSNP: rs3818361
rs3818361
CR1
6 0.851 0.080 1 207611623 intron variant A/G snv 0.74 0.010 1.000 1 2017 2017
dbSNP: rs495490
rs495490
CDKN2B ; CDKN2B-AS1
2 1.000 0.080 9 22010413 intron variant A/G snv 6.8E-02 0.010 1.000 1 2010 2010
dbSNP: rs886205
rs886205
ALDH2
8 0.827 0.360 12 111766623 intron variant A/G snv 0.35 0.010 1.000 1 2010 2010
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
dbSNP: rs997509
rs997509
ENPP1
6 0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 0.010 1.000 1 2009 2009
dbSNP: rs10811661
rs10811661 		22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.010 1.000 1 2011 2011
dbSNP: rs1111875
rs1111875 		10 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 0.010 1.000 1 2014 2014
dbSNP: rs5219
rs5219
KCNJ11
25 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 0.030 1.000 3 2004 2009
dbSNP: rs1042714
rs1042714
ADRB2
54 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 0.010 < 0.001 1 2001 2001
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.040 1.000 4 2000 2012