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: rs62199592
rs62199592 		2 2 183858773 intergenic variant A/G snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs6475417
rs6475417
SLC24A2
2 9 20212043 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6661750
rs6661750
PDE4B
2 1 66081201 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs78809014
rs78809014
MAPKAP1 ; LOC102723468
1 9 125542973 intron variant C/G snv 5.8E-03 2.2E-03 0.010 1.000 1 2019 2019
dbSNP: rs885861
rs885861
VIPR2 ; LINC00689
1 7 159028856 3 prime UTR variant G/A snv 0.43 0.010 1.000 1 2010 2010
dbSNP: rs9316235
rs9316235
HTR2A
2 13 46871568 intron variant G/A snv 0.19 0.010 1.000 1 2010 2010
dbSNP: rs878567
rs878567
HTR1A
4 0.882 0.040 5 63960164 intron variant A/C;G snv 0.020 1.000 2 2010 2013
dbSNP: rs10020288
rs10020288 		2 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs10144845
rs10144845
YLPM1
2 1.000 0.040 14 74771067 intron variant C/T snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10156548
rs10156548 		2 1.000 0.040 9 23318435 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10405382
rs10405382
DPY19L3 ; LOC400684
2 1.000 0.040 19 32405810 5 prime UTR variant C/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs10429537
rs10429537 		2 1.000 0.040 9 23346844 intron variant C/G snv 0.33 0.700 1.000 1 2018 2018
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: 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: 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: 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