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: rs1021070
rs1021070
CHRNB4
1 15 78654521 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs10226228
rs10226228
PDE1C
1 7 32276001 intron variant A/G snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs10259431
rs10259431
PDE1C
1 7 32241785 intron variant C/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs10264177
rs10264177
PDE1C
1 7 32331250 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs1028936
rs1028936
HECTD2-AS1
1 10 91590040 regulatory region variant A/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs10951331
rs10951331
PDE1C
1 7 32314762 intron variant A/G snv 0.22 0.700 1.000 1 2010 2010
dbSNP: rs10958725
rs10958725 		1 8 42669441 intergenic variant T/G snv 0.63 0.700 1.000 1 2010 2010
dbSNP: rs10958726
rs10958726 		1 8 42680766 intergenic variant G/T snv 0.66 0.700 1.000 1 2010 2010
dbSNP: rs11071927
rs11071927 		1 15 66968834 intergenic variant C/A snv 0.85 0.700 1.000 1 2010 2010
dbSNP: rs11072810
rs11072810
MORF4L1
1 15 78839864 intron variant T/C snv 0.49 0.700 1.000 1 2010 2010
dbSNP: rs11205911
rs11205911
RAB3B
1 1 51930640 intron variant A/G snv 0.61 0.700 1.000 1 2010 2010
dbSNP: rs11633519
rs11633519
CHRNB4 ; LOC105370913 ; LOC112268142
1 15 78707210 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs11634628
rs11634628
CHRNB4 ; LOC105370913 ; LOC112268142
1 15 78713237 intron variant G/A snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs11852830
rs11852830
MORF4L1
1 15 78833087 intron variant A/T snv 0.55 0.700 1.000 1 2010 2010
dbSNP: rs12531858
rs12531858
PDE1C
1 7 32300487 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs12540232
rs12540232
PDE1C
1 7 32283349 intron variant T/C snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs12566236
rs12566236
RAB3B
1 1 51931271 intron variant G/T snv 0.61 0.700 1.000 1 2010 2010
dbSNP: rs12588659
rs12588659
EVL
1 14 100121476 intron variant C/A snv 6.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs12595538
rs12595538
MORF4L1
1 15 78862111 intron variant A/T snv 0.36 0.700 1.000 1 2010 2010
dbSNP: rs12899940
rs12899940
CHRNB4 ; LOC105370913 ; LOC112268142
1 15 78709357 intron variant C/T snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs12905641
rs12905641
CHRNB4 ; LOC112268142
1 15 78672020 intron variant C/T snv 0.29 0.700 1.000 1 2010 2010
dbSNP: rs12905740
rs12905740
ADAMTS7
1 15 78790022 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs12910237
rs12910237
CHRNB4 ; LOC112268142
1 15 78663996 intron variant C/T snv 0.27 0.700 1.000 1 2010 2010
dbSNP: rs1304100
rs1304100
BDNF-AS
1 11 27550056 intron variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs1326986
rs1326986
MALRD1
1 10 19640584 intron variant T/C snv 4.1E-02 0.700 1.000 1 2010 2010