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: rs231362
rs231362
KCNQ1 ; KCNQ1OT1
1 1.000 0.080 11 2670241 non coding transcript exon variant A/G snv 0.62 0.840 1.000 10 2010 2019
dbSNP: rs3802177
rs3802177
SLC30A8 ; LOC105375716
5 1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 0.820 1.000 10 2008 2019
dbSNP: rs1552224
rs1552224
ARAP1
4 1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 0.820 1.000 8 2010 2018
dbSNP: rs163184
rs163184
KCNQ1
1 1.000 0.080 11 2825839 intron variant T/G snv 0.40 0.810 1.000 8 2010 2018
dbSNP: rs2283228
rs2283228
KCNQ1
1 1.000 0.080 11 2828300 intron variant A/C snv 0.10 0.760 1.000 8 2009 2017
dbSNP: rs972283
rs972283
LOC105375508
3 1.000 0.080 7 130782095 intergenic variant A/G;T snv 0.840 1.000 8 2010 2016
dbSNP: rs10440833
rs10440833
CDKAL1
1 1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 0.820 1.000 7 2010 2019
dbSNP: rs11257655
rs11257655 		4 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 0.800 1.000 7 2013 2019
dbSNP: rs1359790
rs1359790
LOC105370275
1 1.000 0.080 13 80143021 intergenic variant G/A snv 0.23 0.810 1.000 6 2010 2019
dbSNP: rs151290
rs151290
KCNQ1
2 1.000 0.080 11 2800385 intron variant A/C snv 0.67 0.060 0.833 6 2009 2019
dbSNP: rs2237896
rs2237896
KCNQ1
1 1.000 0.080 11 2837210 intron variant G/A;T snv 0.810 1.000 6 2011 2019
dbSNP: rs243021
rs243021 		1 1.000 0.080 2 60357684 intron variant G/A snv 0.45 0.820 1.000 6 2010 2017
dbSNP: rs516946
rs516946
ANK1 ; MIR486-1
1 1.000 0.080 8 41661730 non coding transcript exon variant T/A;C snv 0.78 0.820 1.000 6 2012 2018
dbSNP: rs7034200
rs7034200
GLIS3
3 1.000 0.080 9 4289050 intron variant C/A;G snv 0.750 1.000 6 2011 2019
dbSNP: rs10886471
rs10886471
GRK5
1 1.000 0.080 10 119389891 intron variant C/T snv 0.39 0.850 1.000 5 2013 2018
dbSNP: rs1113132
rs1113132
EXT2
1 1.000 0.080 11 44231853 intron variant G/C snv 0.24 0.050 0.400 5 2012 2015
dbSNP: rs121434581
rs121434581
SLC2A4
1 1.000 0.080 17 7285729 missense variant G/A;C snv 4.2E-03; 4.0E-06 0.700 1.000 5 1991 2013
dbSNP: rs121913150
rs121913150
INSR
1 1.000 0.080 19 7120707 missense variant C/T snv 8.0E-06 7.0E-06 0.800 1.000 5 1992 2013
dbSNP: rs1535500
rs1535500
KCNK16 ; KCNK17 ; LOC105375047
1 1.000 0.080 6 39316274 missense variant G/T snv 0.51 0.60 0.830 1.000 5 2011 2019
dbSNP: rs17168486
rs17168486
DGKB
5 1.000 0.080 7 14858657 intron variant C/T snv 0.18 0.800 1.000 5 2012 2019
dbSNP: rs1801214
rs1801214
WFS1
1 1.000 0.080 4 6301295 missense variant C/A;G;T snv 0.67 0.810 1.000 5 2010 2018
dbSNP: rs4457053
rs4457053
ZBED3-AS1
1 1.000 0.080 5 77129124 intron variant G/A snv 0.74 0.800 1.000 5 2010 2017
dbSNP: rs7041847
rs7041847
GLIS3
2 1.000 0.080 9 4287466 intron variant A/G snv 0.37 0.820 1.000 5 2011 2019
dbSNP: rs831571
rs831571 		1 1.000 0.080 3 64062621 intergenic variant T/C snv 0.81 0.830 1.000 5 2011 2019
dbSNP: rs10885409
rs10885409
TCF7L2
3 1.000 0.080 10 113048313 intron variant T/C snv 0.54 0.720 1.000 4 2007 2015