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: rs11558471
rs11558471
SLC30A8 ; LOC105375716
5 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 0.800 1.000 6 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: rs2191349
rs2191349 		4 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 0.800 1.000 5 2010 2019
dbSNP: rs10885122
rs10885122 		4 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 0.800 1.000 4 2010 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: rs174550
rs174550
FADS1 ; FADS2
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.800 1.000 4 2010 2015
dbSNP: rs340874
rs340874
PROX1 ; PROX1-AS1
7 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 0.800 1.000 4 2010 2019
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: rs7034200
rs7034200
GLIS3
3 1.000 0.080 9 4289050 intron variant C/A;G snv 0.700 1.000 3 2010 2015
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: rs11071657
rs11071657 		3 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 0.700 1.000 1 2010 2010
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: rs895636
rs895636 		2 2 44961214 non coding transcript exon variant C/T snv 0.23 0.700 1.000 3 2011 2018
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: rs10811661
rs10811661 		22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.800 1.000 5 2012 2015
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 5 2012 2019
dbSNP: rs1483121
rs1483121 		4 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 0.800 1.000 3 2012 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: 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