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: 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: rs10497655
rs10497655
ZNF804A ; LOC105373780
2 1.000 0.040 2 184597314 intron variant T/C;G snv 0.700 1.000 1 2019 2019
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: rs11066453
rs11066453
OAS1
4 1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 0.700 1.000 1 2011 2011
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: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
21 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 0.800 1.000 1 2012 2012
dbSNP: rs1169313
rs1169313
C12orf43
6 12 121004867 intron variant T/A;C snv 0.700 1.000 1 2008 2008
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: rs12145922
rs12145922
PKN2-AS1
2 1 88680551 intron variant C/A snv 0.57 0.800 1.000 1 2011 2011
dbSNP: rs12229654
rs12229654 		20 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs12539316
rs12539316 		6 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs12594627
rs12594627
CD276
1 15 73693923 intron variant G/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 2 2011 2018
dbSNP: rs12968116
rs12968116
ATP8B1 ; LOC100505549
2 18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 0.800 1.000 1 2011 2011