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 4 2007 2013
dbSNP: rs1106683
rs1106683 		3 7 131768766 intergenic variant G/A snv 0.14 0.700 1.000 1 2007 2007
dbSNP: rs17782313
rs17782313 		34 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 0.700 1.000 3 2008 2014
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs16986921
rs16986921
CTNNBL1
3 1.000 0.080 20 37754119 intron variant C/T snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs6013029
rs6013029
CTNNBL1
5 0.882 0.160 20 37771178 intron variant G/T snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs6020712
rs6020712
CTNNBL1
4 1.000 0.080 20 37758210 intron variant G/A snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs7001819
rs7001819
LOC105379243
4 0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 0.700 1.000 1 2008 2008
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.700 1.000 5 2009 2013
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.700 1.000 4 2009 2014
dbSNP: rs7138803
rs7138803 		17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.700 1.000 4 2009 2013
dbSNP: rs2815752
rs2815752
LOC105378797
7 0.925 0.200 1 72346757 intron variant G/A snv 0.62 0.700 1.000 3 2009 2013
dbSNP: rs29941
rs29941 		6 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 0.700 1.000 3 2009 2013
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 3 2009 2013
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.700 1.000 3 2009 2013
dbSNP: rs12970134
rs12970134 		13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.700 1.000 2 2009 2012
dbSNP: rs2568958
rs2568958
LOC105378797
8 0.882 0.160 1 72299433 intron variant G/A;C snv 0.700 1.000 2 2009 2013
dbSNP: rs7498665
rs7498665
SH2B1
9 0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 0.700 1.000 2 2009 2009
dbSNP: rs7561317
rs7561317 		7 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 0.700 1.000 2 2009 2009
dbSNP: rs10173167
rs10173167 		2 2 646767 intergenic variant G/A snv 0.82 0.700 1.000 1 2009 2009
dbSNP: rs10188334
rs10188334 		2 2 653874 regulatory region variant C/A;T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs10193244
rs10193244 		2 2 647580 intergenic variant T/C snv 0.77 0.700 1.000 1 2009 2009
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: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
7 1.000 0.080 1 177944384 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009