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: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.800 1.000 3 2009 2017
dbSNP: rs11152213
rs11152213 		4 1.000 0.080 18 60185715 intergenic variant A/C;T snv 0.800 1.000 2 2009 2019
dbSNP: rs12967135
rs12967135 		8 18 60181790 intergenic variant G/A snv 0.24 0.800 1.000 2 2009 2017
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.800 1.000 2 2009 2019
dbSNP: rs6567160
rs6567160 		12 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 0.800 1.000 2 2009 2015
dbSNP: rs7138803
rs7138803 		17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.800 1.000 2 2009 2015
dbSNP: rs7144011
rs7144011
NRXN3
4 1.000 0.080 14 79474040 intron variant G/T snv 0.21 0.800 1.000 2 2009 2015
dbSNP: rs10146997
rs10146997
NRXN3
6 0.827 0.240 14 79478819 intron variant A/G snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs1440072
rs1440072
KCNE4
1 2 223072020 intron variant C/A;G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs2075064
rs2075064
LHX2
1 9 124021568 intron variant C/T snv 0.35 0.800 1.000 1 2013 2013
dbSNP: rs2570467
rs2570467
LOC101929710
1 5 96520975 intron variant A/G snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs4471028
rs4471028
GDAP1
1 8 74382740 intron variant T/G snv 0.36 0.800 1.000 1 2007 2007
dbSNP: rs489693
rs489693 		2 1.000 0.080 18 60215554 intergenic variant C/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs6867983
rs6867983
C5orf67
1 5 56558326 intron variant C/T snv 0.17 0.800 1.000 1 2013 2013
dbSNP: rs7601155
rs7601155
BABAM2
1 2 28124815 intron variant C/T snv 6.8E-02 0.800 1.000 1 2013 2013
dbSNP: rs10051787
rs10051787
CEP120
1 5 123396542 intron variant T/C snv 0.73 0.700 1.000 1 2016 2016
dbSNP: rs10132280
rs10132280 		6 14 25458973 intergenic variant C/A snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs10145154
rs10145154
NRXN3
1 14 79473182 intron variant C/T snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs10150332
rs10150332
NRXN3
4 14 79470621 intron variant T/C snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs1062070
rs1062070
RNF5 ; MIR6833
1 6 32180254 synonymous variant A/G snv 0.13 0.14 0.700 1.000 1 2019 2019
dbSNP: rs10767654
rs10767654
BDNF-AS ; LINC00678
2 11 27618676 intron variant T/G snv 0.73 0.700 1.000 1 2017 2017
dbSNP: rs10767658
rs10767658
BDNF-AS
2 11 27650705 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10840100
rs10840100
TRIM66
2 11 8647890 intron variant A/G snv 0.59 0.700 1.000 1 2015 2015
dbSNP: rs10852521
rs10852521
FTO
2 1.000 0.080 16 53771053 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10871777
rs10871777 		6 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 0.700 1.000 1 2009 2009