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: rs2166706
rs2166706 		2 1.000 0.080 11 92958366 intergenic variant T/A;C snv 0.800 1.000 2 2009 2019
dbSNP: rs2268575
rs2268575
GCK ; LOC105375258
2 7 44149675 intron variant T/C snv 0.18 0.800 1.000 2 2012 2019
dbSNP: rs2877716
rs2877716
ADCY5
4 3 123375604 intron variant T/C snv 0.76 0.800 1.000 2 2012 2012
dbSNP: rs3802177
rs3802177
SLC30A8 ; LOC105375716
5 1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 0.800 1.000 2 2012 2015
dbSNP: rs4237150
rs4237150
GLIS3
2 9 4290085 intron variant G/A;C;T snv 0.800 1.000 2 2012 2015
dbSNP: rs6113722
rs6113722
LINC00261
2 20 22576461 intron variant G/A;T snv 0.800 1.000 2 2012 2019
dbSNP: rs853789
rs853789
ABCB11
4 2 168944978 intron variant A/G;T snv 0.75 0.800 1.000 2 2012 2018
dbSNP: rs2722425
rs2722425
ZMAT4
1 8 40626720 intron variant T/C snv 0.78 0.800 1.000 1 2007 2007
dbSNP: rs563694
rs563694
ABCB11
2 2 168917561 intron variant C/A snv 0.75 0.800 1.000 1 2008 2008
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