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: rs1049353
rs1049353
CNR1
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2010 2010
dbSNP: rs1055447
rs1055447
C11orf49 ; ARFGAP2
2 1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10748842
rs10748842
NRG3
8 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs10868235
rs10868235
NTRK2
6 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs10891564
rs10891564 		2 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs10950393
rs10950393
TMEM106B
2 1.000 0.040 7 12223920 intron variant T/C snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10965780
rs10965780 		3 1.000 0.040 9 23341717 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10994336
rs10994336
ANK3
12 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 0.010 1.000 1 2014 2014
dbSNP: rs11039149
rs11039149
NR1H3
6 0.827 0.280 11 47255124 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs11039409
rs11039409
NUP160
2 1.000 0.040 11 47814169 intron variant A/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs11123857
rs11123857
NPAS2
2 2 100987350 non coding transcript exon variant A/G snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs111365677
rs111365677 		3 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs11152363
rs11152363
TCF4
2 1.000 0.040 18 55389957 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11209175
rs11209175
GNG12-AS1
2 1.000 0.040 1 67909145 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs112106319
rs112106319
TNC ; DELEC1
3 0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs11214589
rs11214589
TTC12
2 1.000 0.040 11 113374326 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs11214607
rs11214607
DRD2
2 1.000 0.040 11 113441417 intron variant T/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs112538845
rs112538845 		3 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs113378111
rs113378111 		3 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs114465512
rs114465512
IGLV10-54
3 1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 0.700 1.000 1 2016 2016
dbSNP: rs11514731
rs11514731
MAD1L1
2 1.000 0.040 7 2011868 intron variant C/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11599236
rs11599236
SORCS3
2 1.000 0.040 10 104694914 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs11605020
rs11605020
LOC105369562
2 1.000 0.040 11 127110970 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11608355
rs11608355
MYO1H
2 1.000 0.040 12 109441487 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs116362708
rs116362708
SLC44A5
2 1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 0.700 1.000 1 2018 2018