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: rs10018902
rs10018902 		2 4 120941346 intergenic variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10198628
rs10198628 		2 2 12824371 intron variant A/G snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs1056513
rs1056513
PATJ
3 1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs10782199
rs10782199
LOC105377975
1 6 119791894 intergenic variant G/A snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
7 1.000 0.080 1 177944384 intron variant T/C snv 0.22 0.800 1.000 1 2009 2009
dbSNP: rs11030102
rs11030102
BDNF ; BDNF-AS
2 11 27660049 non coding transcript exon variant C/G snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs112037309
rs112037309
ARHGEF38 ; INTS12
1 4 105695979 intron variant G/A snv 6.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs112540634
rs112540634
ILRUN
2 6 34656128 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs113191842
rs113191842
FTO
5 16 53783406 intron variant G/A snv 9.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs116975424
rs116975424
RFX3
2 9 3518833 intron variant T/C snv 2.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs11847697
rs11847697
PRKD1
5 14 30045906 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs11863065
rs11863065 		3 16 82293200 intergenic variant G/A snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs12146733
rs12146733
FAIM2
3 12 49876581 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12517906
rs12517906 		1 5 180743819 upstream gene variant C/A;T snv 0.11 0.800 1.000 1 2010 2010
dbSNP: rs12625495
rs12625495
ZNF341
2 20 33775731 intron variant G/A;C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12705992
rs12705992 		1 7 114789947 regulatory region variant G/A snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs12967135
rs12967135 		8 18 60181790 intergenic variant G/A snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs12970134
rs12970134 		13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.800 1.000 1 2009 2009
dbSNP: rs13029479
rs13029479 		1 2 655222 regulatory region variant G/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs143384
rs143384
GDF5
17 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs146144484
rs146144484 		2 6 3865792 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs1650505
rs1650505 		2 5 158602726 intergenic variant G/A snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs16877106
rs16877106
ANAPC4
1 4 25401644 intron variant C/T snv 4.9E-02 0.800 1.000 1 2011 2011
dbSNP: rs17109221
rs17109221
NRXN3
1 14 79443776 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017