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: rs147914600
rs147914600
SYT3
1 19 50637155 intron variant C/T snv 3.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs1549293
rs1549293
KAT8
1 16 31130672 3 prime UTR variant C/T snv 0.31 0.700 1.000 1 2015 2015
dbSNP: rs1559318
rs1559318 		1 16 26805992 intergenic variant C/A snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs16894959
rs16894959
UHRF1BP1
2 6 34857885 synonymous variant T/C snv 0.13 0.18 0.700 1.000 1 2015 2015
dbSNP: rs16996700
rs16996700
LINC01524 ; LOC105372666
3 20 52365406 intron variant T/C snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs17075725
rs17075725
GRM1
1 6 146194776 intron variant G/A snv 1.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs17109256
rs17109256
NRXN3
3 14 79473650 intron variant G/A snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs17309874
rs17309874
BDNF-AS
1 11 27645689 intron variant G/A snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs184622626
rs184622626
ZMAT4
1 8 40782400 intron variant A/C snv 2.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs1868673
rs1868673 		1 3 150469527 downstream gene variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs190051860
rs190051860
LOC101928135
1 3 35156031 intergenic variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs1916799
rs1916799
FHIT
3 3 61247301 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2033529
rs2033529
TDRG1
4 6 40380914 intron variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs2075064
rs2075064
LHX2
1 9 124021568 intron variant C/T snv 0.35 0.800 1.000 1 2013 2013
dbSNP: rs2168711
rs2168711 		1 18 60181298 intergenic variant T/C snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs2176040
rs2176040 		3 2 226228086 intergenic variant A/G snv 0.67 0.700 1.000 1 2015 2015
dbSNP: rs2222328
rs2222328
SCHIP1 ; IQCJ-SCHIP1
2 3 159541502 intron variant T/C snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs2272805
rs2272805
RIBC2 ; SMC1B
1 22 45413817 5 prime UTR variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs2293576
rs2293576
SLC39A13
2 11 47413435 synonymous variant G/A;T snv 0.31; 4.0E-06 0.700 1.000 1 2015 2015
dbSNP: rs2325036
rs2325036
CADM2
1 3 85770262 intron variant A/C snv 0.41 0.700 1.000 1 2015 2015
dbSNP: rs2489623
rs2489623
RSPO3
2 6 127134676 intron variant A/C snv 0.55 0.700 1.000 1 2015 2015
dbSNP: rs2531992
rs2531992
ADCY9
2 16 3971733 intron variant A/G snv 0.80 0.700 1.000 1 2015 2015
dbSNP: rs2570467
rs2570467
LOC101929710
1 5 96520975 intron variant A/G snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs2650492
rs2650492
SBK1
5 16 28322090 3 prime UTR variant G/A snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs2820292
rs2820292
NAV1 ; IPO9-AS1
3 1 201815159 intron variant A/C snv 0.48 0.700 1.000 1 2015 2015