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: rs9292468
rs9292468 		6 5 32818967 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs9286060
rs9286060 		2 8 9795635 intergenic variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9266359
rs9266359 		1 6 31364962 upstream gene variant C/T snv 0.22 0.700 1.000 1 2015 2015
dbSNP: rs926552
rs926552
GABBR1 ; SNORD32B
1 6 29580312 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs925946
rs925946
BDNF-AS
9 0.882 0.120 11 27645655 intron variant T/G snv 0.72 0.700 1.000 1 2016 2016
dbSNP: rs919045
rs919045
DCDC1
1 11 31090263 intron variant T/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs918466
rs918466
ADAMTS9-AS2
1 3 64724577 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs903432
rs903432
PDE10A
2 6 165761983 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs900145
rs900145 		4 11 13272358 upstream gene variant C/T snv 0.62 0.700 1.000 3 2016 2018
dbSNP: rs893929
rs893929 		3 4 143266227 intergenic variant G/A snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs891511
rs891511
NOS3
4 7 151007755 intron variant G/A;C snv 0.700 1.000 2 2016 2019
dbSNP: rs890431
rs890431
HOXB7
3 17 48609478 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs888987
rs888987
EBF1
2 5 159021393 intron variant G/C snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs880315
rs880315
CASZ1
9 0.925 0.120 1 10736809 intron variant T/C snv 0.32 0.700 1.000 9 2011 2018
dbSNP: rs875589
rs875589 		1 13 72700734 upstream gene variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs875106
rs875106
ANO1
1 11 70159535 intron variant G/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs873122
rs873122
SLCO3A1
1 15 92158790 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs871606
rs871606 		3 4 53933078 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs867186
rs867186
PROCR ; MMP24-AS1-EDEM2
15 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs850892
rs850892 		1 2 185344583 intergenic variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs8139817
rs8139817
MICAL3
1 22 17985603 intron variant A/C snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs8105753
rs8105753 		2 19 31436641 regulatory region variant A/C snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs8098380
rs8098380
YES1
4 18 721563 downstream gene variant A/C snv 0.33 0.700 1.000 2 2018 2018
dbSNP: rs8084192
rs8084192
YES1
1 18 753630 intron variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs8082812
rs8082812 		16 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 0.700 1.000 1 2016 2016