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: rs1497406
rs1497406 		1 1 16178825 intergenic variant A/G snv 0.47 0.800 1.000 3 2011 2019
dbSNP: rs4074793
rs4074793
ITGA1
1 5 52897294 intron variant A/G snv 6.6E-02 0.800 1.000 2 2011 2018
dbSNP: rs4581712
rs4581712
LOC102724084
1 16 80463704 intron variant C/A snv 0.22 0.800 1.000 2 2011 2018
dbSNP: rs10458877
rs10458877
LINC02682
1 11 15919553 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs10460702
rs10460702
LOC105372767
1 21 29182833 intron variant G/A snv 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs10513686
rs10513686
SLC2A2
1 3 171007753 intron variant G/A snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs1076540
rs1076540
MICAL3
1 22 17957192 intron variant C/T snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs10908458
rs10908458 		1 1 155154472 intergenic variant T/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs10913568
rs10913568
TEX35 ; C1orf220
1 1 178544276 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs10917347
rs10917347
KDM1A
1 1 23050048 intron variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs10919882
rs10919882
LINC00862
1 1 200291886 intron variant C/A snv 7.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs11002319
rs11002319
DLG5
1 10 77876403 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs111804060
rs111804060
NUP210L
1 1 154114036 intron variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs1126617
rs1126617
GPLD1
1 6 24489424 missense variant C/T snv 0.29 0.31 0.700 1.000 1 2011 2011
dbSNP: rs115231893
rs115231893 		1 22 24688848 downstream gene variant G/A snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs117322666
rs117322666
SLC24A2
1 9 19586969 intron variant T/G snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs117791138
rs117791138 		1 12 24965415 downstream gene variant A/G snv 2.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs11830764
rs11830764
CUX2
1 12 111077216 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12594627
rs12594627
CD276
1 15 73693923 intron variant G/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs13030978
rs13030978
MYO1B
1 2 191252512 intron variant C/T snv 0.24 0.800 1.000 1 2011 2011
dbSNP: rs13084607
rs13084607
ARPP21
1 3 35736301 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs13289095
rs13289095
PKN3
1 9 128704210 intron variant G/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs1335645
rs1335645
CEPT1 ; DRAM2
1 1 111141654 intron variant A/G;T snv 0.15 0.800 1.000 1 2011 2011
dbSNP: rs138871903
rs138871903 		1 14 103348238 downstream gene variant C/T snv 7.3E-04 0.700 1.000 1 2018 2018
dbSNP: rs1392428
rs1392428 		1 5 31024746 intergenic variant T/C snv 0.23 0.700 1.000 1 2018 2018