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 0.700 1.000 6 2007 2019
dbSNP: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 2 2007 2019
dbSNP: rs1106683
rs1106683 		3 7 131768766 intergenic variant G/A snv 0.14 0.700 1.000 1 2007 2007
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 3 2008 2019
dbSNP: rs17782313
rs17782313 		34 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 0.700 1.000 3 2008 2017
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.700 1.000 14 2009 2019
dbSNP: rs7138803
rs7138803 		17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.700 1.000 12 2009 2019
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.700 1.000 7 2009 2019
dbSNP: rs29941
rs29941 		6 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 0.700 1.000 6 2009 2018
dbSNP: rs7647305
rs7647305
DGKG
8 1.000 0.080 3 186116501 intron variant T/C snv 0.74 0.700 1.000 5 2009 2019
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.800 1.000 5 2009 2019
dbSNP: rs7498665
rs7498665
SH2B1
9 0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 0.700 1.000 4 2009 2019
dbSNP: rs2568958
rs2568958
LOC105378797
8 0.882 0.160 1 72299433 intron variant G/A;C snv 0.700 1.000 3 2009 2019
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
7 1.000 0.080 1 177944384 intron variant T/C snv 0.22 0.700 1.000 2 2009 2019
dbSNP: rs2815752
rs2815752
LOC105378797
7 0.925 0.200 1 72346757 intron variant G/A snv 0.62 0.700 1.000 2 2009 2010
dbSNP: rs6548238
rs6548238 		10 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 0.700 1.000 2 2009 2019
dbSNP: rs7561317
rs7561317 		7 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 0.700 1.000 2 2009 2019
dbSNP: rs10769908
rs10769908
STK33
4 11 8462542 intron variant C/T snv 0.55 0.700 1.000 1 2009 2009
dbSNP: rs10838738
rs10838738
MTCH2
6 1.000 0.080 11 47641497 intron variant A/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs11084753
rs11084753 		6 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 0.700 1.000 1 2009 2009
dbSNP: rs12970134
rs12970134 		13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs6499640
rs6499640
FTO
7 0.925 0.160 16 53735765 intron variant G/A snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs925946
rs925946
BDNF-AS
9 0.882 0.120 11 27645655 intron variant T/G snv 0.72 0.700 1.000 1 2009 2009
dbSNP: rs543874
rs543874 		11 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 0.700 1.000 14 2010 2019
dbSNP: rs13107325
rs13107325
SLC39A8
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 11 2010 2019