Source: GWASDB ×
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
6 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.800 1.000 3 2009 2019
dbSNP: rs1387153
rs1387153 		4 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 0.800 1.000 3 2009 2019
dbSNP: rs4607517
rs4607517
GCK
3 0.882 0.080 7 44196069 intron variant G/A;C snv 0.800 1.000 3 2009 2019
dbSNP: rs560887
rs560887
SPC25 ; G6PC2
7 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 0.800 1.000 3 2008 2019
dbSNP: rs7903146
rs7903146
TCF7L2
8 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 3 2009 2019
dbSNP: rs10811661
rs10811661 		4 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.800 1.000 2 2012 2015
dbSNP: rs10885122
rs10885122 		3 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 0.800 1.000 1 2010 2019
dbSNP: rs11039182
rs11039182
MADD
2 11 47325172 intron variant T/C snv 0.19 0.800 1.000 1 2012 2019
dbSNP: rs11558471
rs11558471
SLC30A8 ; LOC105375716
5 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 0.800 1.000 1 2010 2019
dbSNP: rs11603334
rs11603334
ARAP1
4 1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs11605924
rs11605924
CRY2
3 1.000 0.080 11 45851540 intron variant A/C snv 0.39 0.800 1.000 1 2010 2019
dbSNP: rs11619319
rs11619319
PLUT
2 13 27913462 intron variant A/G snv 0.23 0.800 1.000 1 2012 2015
dbSNP: rs11708067
rs11708067
ADCY5
4 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.800 1.000 1 2010 2019
dbSNP: rs11920090
rs11920090
SLC2A2
3 1.000 0.040 3 170999732 intron variant T/A snv 0.20 0.800 1.000 1 2010 2015
dbSNP: rs1260326
rs1260326
GCKR
25 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 1 2012 2019
dbSNP: rs1371614
rs1371614
DPYSL5
3 2 26930006 intron variant C/T snv 0.29 0.800 1.000 1 2012 2012
dbSNP: rs1483121
rs1483121 		3 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 0.800 1.000 1 2012 2019
dbSNP: rs17265513
rs17265513
ZHX3
2 0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 0.800 1.000 1 2012 2015
dbSNP: rs174550
rs174550
FADS1 ; FADS2
6 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.800 1.000 1 2010 2015
dbSNP: rs1799884
rs1799884
GCK
4 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.800 1.000 1 2011 2019
dbSNP: rs2166706
rs2166706 		1 1.000 0.080 11 92958366 intergenic variant T/A;C snv 0.800 1.000 1 2009 2019
dbSNP: rs2191349
rs2191349 		4 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 0.800 1.000 1 2010 2019
dbSNP: rs2268575
rs2268575
GCK ; LOC105375258
2 7 44149675 intron variant T/C snv 0.18 0.800 1.000 1 2012 2019
dbSNP: rs2722425
rs2722425
ZMAT4
1 8 40626720 intron variant T/C snv 0.78 0.800 1.000 1 2007 2007
dbSNP: rs2877716
rs2877716
ADCY5
3 3 123375604 intron variant T/C snv 0.76 0.800 1.000 1 2012 2012