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: rs10830963
rs10830963
MTNR1B
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.800 1.000 11 2009 2019
dbSNP: rs560887
rs560887
SPC25 ; G6PC2
18 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 9 2008 2019
dbSNP: rs4607517
rs4607517
GCK
8 0.882 0.080 7 44196069 intron variant G/A;C snv 0.800 1.000 7 2009 2019
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 7 2010 2019
dbSNP: rs11708067
rs11708067
ADCY5
9 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.800 1.000 5 2010 2019
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 5 2009 2019
dbSNP: rs11605924
rs11605924
CRY2
5 1.000 0.080 11 45851540 intron variant A/C snv 0.39 0.800 1.000 4 2010 2019
dbSNP: rs11920090
rs11920090
SLC2A2
5 1.000 0.040 3 170999732 intron variant T/A snv 0.20 0.800 1.000 4 2010 2015
dbSNP: rs4506565
rs4506565
TCF7L2
22 0.790 0.280 10 112996282 intron variant A/G;T snv 0.800 1.000 4 2010 2019
dbSNP: rs7944584
rs7944584
MADD
5 1.000 0.080 11 47314769 intron variant A/T snv 0.19 0.800 1.000 4 2010 2015
dbSNP: rs16856247
rs16856247
ABCB11
2 2 168927903 intron variant C/T snv 6.6E-02 0.700 1.000 3 2011 2019
dbSNP: rs1799884
rs1799884
GCK
6 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.800 1.000 3 2011 2019
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: rs11039182
rs11039182
MADD
2 11 47325172 intron variant T/C snv 0.19 0.800 1.000 2 2012 2019
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: 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: 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: 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