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: 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: rs11039182
rs11039182
MADD
2 11 47325172 intron variant T/C snv 0.19 0.800 1.000 2 2012 2019
dbSNP: rs11603334
rs11603334
ARAP1
5 1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 0.800 1.000 2 2012 2012
dbSNP: rs11619319
rs11619319
PLUT
2 13 27913462 intron variant A/G snv 0.23 0.800 1.000 2 2012 2015
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: rs1371614
rs1371614
DPYSL5
3 2 26930006 intron variant C/T snv 0.29 0.800 1.000 2 2012 2012
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: rs17265513
rs17265513
ZHX3
6 0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 0.800 1.000 2 2012 2015
dbSNP: rs1974620
rs1974620 		2 1.000 0.080 7 15025842 intergenic variant C/A;T snv 0.700 1.000 2 2015 2019
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: rs3847554
rs3847554 		1 11 92935660 upstream gene variant C/T snv 0.56 0.700 1.000 2 2015 2019
dbSNP: rs4237150
rs4237150
GLIS3
2 9 4290085 intron variant G/A;C;T snv 0.800 1.000 2 2012 2015
dbSNP: rs6048216
rs6048216
LNCNEF
1 20 22600630 intron variant T/C snv 0.17 0.700 1.000 2 2015 2019
dbSNP: rs6113722
rs6113722
LINC00261
2 20 22576461 intron variant G/A;T snv 0.800 1.000 2 2012 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: rs853789
rs853789
ABCB11
4 2 168944978 intron variant A/G;T snv 0.75 0.800 1.000 2 2012 2018
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