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: rs12444979
rs12444979
LOC105371116
4 1.000 0.080 16 19922278 intergenic variant C/T snv 0.11 0.700 1.000 2 2010 2013
dbSNP: rs12463617
rs12463617 		4 1.000 0.080 2 629244 regulatory region variant A/C;T snv 0.700 1.000 2 2013 2014
dbSNP: rs12597579
rs12597579 		3 16 20246545 intergenic variant C/A;T snv 0.700 1.000 2 2012 2014
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: rs13078807
rs13078807
CADM2
5 0.925 0.120 3 85835000 intron variant A/G snv 0.15 0.700 1.000 2 2010 2013
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 2 2010 2013
dbSNP: rs1555543
rs1555543 		3 1 96479241 intergenic variant A/C snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs2030323
rs2030323
BDNF
6 0.925 0.080 11 27706992 intron variant A/C snv 0.83 0.700 1.000 2 2012 2013
dbSNP: rs206936
rs206936
NUDT3 ; RPS10-NUDT3
8 0.882 0.160 6 34335092 intron variant A/G snv 0.34 0.700 1.000 2 2010 2013
dbSNP: rs2112347
rs2112347
POC5 ; LOC441087
10 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 0.700 1.000 2 2010 2013
dbSNP: rs2287019
rs2287019
QPCTL
7 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 0.700 1.000 2 2010 2013
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: rs261967
rs261967
LOC101929710 ; LOC107986362
3 5 96514546 intron variant A/C snv 0.42 0.700 1.000 2 2012 2014
dbSNP: rs2890652
rs2890652 		3 2 142202362 intergenic variant T/C snv 0.21 0.700 1.000 2 2010 2013
dbSNP: rs3817334
rs3817334
MTCH2
7 1.000 0.080 11 47629441 intron variant C/T snv 0.36 0.700 1.000 2 2010 2013
dbSNP: rs4771122
rs4771122
MTIF3
4 1.000 0.080 13 27446043 intron variant G/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs4776970
rs4776970
MAP2K5
4 15 67788548 intron variant A/T snv 0.44 0.700 1.000 2 2012 2014
dbSNP: rs4836133
rs4836133
LINC02240 ; LOC105379158
5 0.925 0.160 5 124996410 intron variant C/A;G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs4929949
rs4929949
STK33
4 1.000 0.080 11 8583046 intron variant T/C snv 0.46 0.700 1.000 2 2010 2013
dbSNP: rs571312
rs571312 		7 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 0.700 1.000 2 2010 2013
dbSNP: rs574367
rs574367 		3 1 177904075 intron variant G/T snv 0.16 0.700 1.000 2 2012 2014
dbSNP: rs6545814
rs6545814
ADCY3
3 2 24908447 intron variant A/G snv 0.53 0.700 1.000 2 2012 2014
dbSNP: rs713586
rs713586 		5 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 0.700 1.000 2 2010 2013
dbSNP: rs7359397
rs7359397
SH2B1
5 1.000 0.040 16 28874338 upstream gene variant C/T snv 0.28 0.700 1.000 2 2010 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