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: rs16856247
rs16856247
ABCB11
2 2 168927903 intron variant C/T snv 6.6E-02 0.700 1.000 3 2011 2019
dbSNP: rs4841132
rs4841132
LOC157273
14 8 9326086 non coding transcript exon variant A/G snv 0.89 0.700 1.000 3 2012 2015
dbSNP: rs7034200
rs7034200
GLIS3
3 1.000 0.080 9 4289050 intron variant C/A;G snv 0.700 1.000 3 2010 2015
dbSNP: rs895636
rs895636 		2 2 44961214 non coding transcript exon variant C/T snv 0.23 0.700 1.000 3 2011 2018
dbSNP: rs10305492
rs10305492
GLP1R ; LOC105375046
2 1.000 0.080 6 39079018 missense variant G/A snv 1.0E-02 1.1E-02 0.700 1.000 2 2015 2015
dbSNP: rs10830962
rs10830962 		7 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 0.700 1.000 2 2011 2019
dbSNP: rs11717195
rs11717195
ADCY5
3 1.000 0.080 3 123363551 intron variant T/C snv 0.19 0.700 1.000 2 2012 2012
dbSNP: rs1209523
rs1209523
FOXA2 ; LNCNEF
2 1.000 0.080 20 22587304 upstream gene variant C/T snv 0.14 0.700 1.000 2 2010 2019
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
23 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 0.700 1.000 2 2015 2017
dbSNP: rs13387347
rs13387347
SPC25
1 2 168898336 intron variant T/C snv 0.49 0.700 1.000 2 2015 2018
dbSNP: rs17168486
rs17168486
DGKB
5 1.000 0.080 7 14858657 intron variant C/T snv 0.18 0.700 1.000 2 2012 2012
dbSNP: rs1974620
rs1974620 		2 1.000 0.080 7 15025842 intergenic variant C/A;T snv 0.700 1.000 2 2015 2019
dbSNP: rs3847554
rs3847554 		1 11 92935660 upstream gene variant C/T snv 0.56 0.700 1.000 2 2015 2019
dbSNP: rs6048216
rs6048216
LNCNEF
1 20 22600630 intron variant T/C snv 0.17 0.700 1.000 2 2015 2019
dbSNP: rs730497
rs730497
GCK ; LOC105375257
4 0.882 0.160 7 44184122 intron variant G/A snv 0.17 0.700 1.000 2 2015 2019
dbSNP: rs7936247
rs7936247 		5 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 0.700 1.000 2 2013 2019
dbSNP: rs10228456
rs10228456 		3 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs10246797
rs10246797
SUGCT
1 7 40304762 intron variant C/A;G snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs10248619
rs10248619
GRB10
2 7 50683393 intron variant T/C snv 0.71 0.700 1.000 1 2012 2012
dbSNP: rs10259649
rs10259649
GCK ; LOC105375257
1 7 44180106 intron variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10276674
rs10276674
DGKB
1 7 14882382 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10278336
rs10278336
YKT6
2 7 44205764 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10497345
rs10497345
SPC25
1 2 168878291 intron variant G/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10500292
rs10500292
SYMPK
2 19 45824675 intron variant C/T snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs10501320
rs10501320
MADD ; MADD-AS1
5 0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 0.700 1.000 1 2019 2019