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: rs219781
rs219781
CLDN14 ; LOC105369301
2 1.000 0.120 21 36460323 non coding transcript exon variant G/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs34861762
rs34861762 		3 1.000 0.080 8 23890907 regulatory region variant C/T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs35258188
rs35258188
WDR72
4 1.000 0.040 15 53705141 missense variant T/G snv 3.5E-03 1.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs35612982
rs35612982
CDKAL1
2 1.000 0.080 6 20682391 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs3925584
rs3925584
LOC101928338
7 1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs4148152
rs4148152
ABCG2
2 1.000 0.040 4 88139757 intron variant T/C snv 0.11 7.1E-02 0.700 1.000 1 2014 2014
dbSNP: rs4805497
rs4805497 		2 1.000 0.080 19 29914778 upstream gene variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs61754122
rs61754122
BCAS1
3 1.000 0.040 20 54028628 missense variant C/A;T snv 1.1E-02; 8.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs62416056
rs62416056
GJA10
2 1.000 0.080 6 89918054 intron variant G/C snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs62435145
rs62435145 		8 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs6928482
rs6928482
HLA-DQB1-AS1
3 1.000 0.120 6 32658472 upstream gene variant T/C snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs703978
rs703978
ZMIZ1
3 1.000 0.080 10 79184390 intron variant C/G;T snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs73728279
rs73728279
PRKAG2
4 1.000 0.080 7 151714408 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs753725
rs753725
VARS2
2 1.000 0.120 6 30923094 intron variant T/C snv 0.61 0.51 0.700 1.000 1 2019 2019
dbSNP: rs7678287
rs7678287
SLC2A9 ; LOC105374476
2 1.000 0.080 4 9998877 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs76909566
rs76909566
NFIC
2 1.000 0.080 19 3456658 intron variant G/A snv 0.12 0.11 0.700 1.000 1 2018 2018
dbSNP: rs77924615
rs77924615
PDILT
7 1.000 0.080 16 20381010 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs78260152
rs78260152
LINC01721
2 1.000 0.080 20 24146125 intron variant C/T snv 5.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs9271585
rs9271585 		2 1.000 0.040 6 32623102 regulatory region variant C/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs9379832
rs9379832 		3 1.000 0.080 6 26185972 downstream gene variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs13129697
rs13129697
SLC2A9
5 0.925 0.120 4 9925343 intron variant T/G snv 0.39 0.800 1.000 6 2009 2018
dbSNP: rs2078267
rs2078267
SLC22A11
3 0.925 0.120 11 64566642 non coding transcript exon variant C/T snv 0.37 0.800 1.000 6 2009 2019
dbSNP: rs1471633
rs1471633 		3 0.925 0.120 1 145711327 upstream gene variant T/G snv 0.43 0.800 1.000 3 2009 2019
dbSNP: rs2307394
rs2307394
ORC4
3 0.925 0.120 2 147958859 missense variant T/A;C;G snv 0.36; 8.4E-06 0.700 1.000 3 2013 2019
dbSNP: rs7442295
rs7442295
SLC2A9
5 0.925 0.120 4 9964756 intron variant A/G snv 0.28 0.800 1.000 3 2008 2009