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: rs56135409
rs56135409 		1 1.000 0.040 3 20683524 intron variant C/A snv 0.27 0.700 1.000 3 2018 2019
dbSNP: rs11568324
rs11568324
SLC6A2
1 1.000 0.040 16 55692146 intron variant C/T snv 5.3E-03 0.020 1.000 2 2008 2008
dbSNP: rs1278352
rs1278352
ADAM12
1 1.000 0.040 10 126084807 intron variant A/G snv 0.61 0.700 1.000 2 2016 2016
dbSNP: rs1566652
rs1566652
SLC6A2
1 1.000 0.040 16 55697663 intron variant G/T snv 0.29 0.020 1.000 2 2015 2019
dbSNP: rs1880867
rs1880867
SYT1
1 1.000 0.040 12 79203668 intron variant G/T snv 0.70 0.020 1.000 2 2017 2018
dbSNP: rs36011
rs36011
SLC6A2
1 1.000 0.040 16 55697132 intron variant G/A snv 3.6E-02 0.020 1.000 2 2015 2019
dbSNP: rs763131939
rs763131939
SLC6A3
1 1.000 0.040 5 1394755 missense variant G/A snv 8.0E-06 2.8E-05 0.020 1.000 2 2012 2015
dbSNP: rs8636
rs8636
SNAP25 ; SNAP25-AS1
1 1.000 0.040 20 10307094 3 prime UTR variant T/A;C snv 0.020 1.000 2 2012 2017
dbSNP: rs875342
rs875342
STX1A
1 1.000 0.040 7 73712768 intron variant G/A snv 2.1E-02 0.020 1.000 2 2015 2019
dbSNP: rs10001410
rs10001410
ADGRL3
1 1.000 0.040 4 61608511 intron variant C/A snv 0.55 0.010 1.000 1 2019 2019
dbSNP: rs1049522
rs1049522
SLC1A3
1 1.000 0.040 5 36686784 3 prime UTR variant A/C snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs10514604
rs10514604
ATP2C2
1 1.000 0.040 16 84412778 intron variant C/A;G snv 0.800 1.000 1 2008 2008
dbSNP: rs10762524
rs10762524
PRKG1
1 1.000 0.040 10 52014152 intron variant T/A;C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs10823964
rs10823964
PRKG1
1 1.000 0.040 10 52017283 intron variant T/G snv 0.51 0.700 1.000 1 2010 2010
dbSNP: rs10823973
rs10823973
PRKG1
1 1.000 0.040 10 52019720 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10826548
rs10826548 		1 1.000 0.040 10 28966665 intergenic variant C/A snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs10891819
rs10891819
CADM1
1 1.000 0.040 11 115266527 intron variant T/G snv 0.33 0.010 1.000 1 2019 2019
dbSNP: rs10910623
rs10910623
MAP10
1 1.000 0.040 1 232802953 upstream gene variant G/A snv 7.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs10983238
rs10983238
ASTN2 ; LOC107987015
1 1.000 0.040 9 116571404 intron variant C/A;G snv 0.16 0.800 1.000 1 2008 2008
dbSNP: rs11074889
rs11074889
EMP2
1 1.000 0.040 16 10539308 intron variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs11122330
rs11122330
DISC1 ; TSNAX-DISC1
1 1.000 0.040 1 231762845 intron variant A/G snv 0.14 0.010 1.000 1 2013 2013
dbSNP: rs11243897
rs11243897
AK8
1 1.000 0.040 9 132742896 intron variant A/G snv 0.33 0.800 1.000 1 2008 2008
dbSNP: rs112984125
rs112984125
ST3GAL3 ; KDM4A-AS1
1 1.000 0.040 1 43707752 intron variant G/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs11317767
rs11317767
LOC105371529
1 1.000 0.040 17 8770824 intergenic variant TTT/-;TT;TTTT delins 0.700 1.000 1 2018 2018
dbSNP: rs113828117
rs113828117
DRD5 ; SLC2A9
1 1.000 0.040 4 9783008 missense variant G/A snv 7.0E-06 0.010 1.000 1 2016 2016