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: rs1183910
rs1183910
HNF1A
5 1.000 0.080 12 120983004 intron variant G/A snv 0.28 0.800 1.000 6 2009 2019
dbSNP: rs1341665
rs1341665 		2 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 0.800 1.000 6 2012 2019
dbSNP: rs12068753
rs12068753 		2 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 0.800 1.000 5 2012 2015
dbSNP: rs6734238
rs6734238 		8 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 0.800 1.000 5 2011 2019
dbSNP: rs876537
rs876537
CRPP1
3 1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 0.800 1.000 4 2012 2019
dbSNP: rs11265260
rs11265260 		2 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 0.800 1.000 3 2012 2019
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.800 1.000 3 2011 2019
dbSNP: rs1160985
rs1160985
TOMM40
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.800 1.000 2 2012 2019
dbSNP: rs1169286
rs1169286
HNF1A
3 1.000 0.080 12 120981253 intron variant T/C snv 0.39 0.700 1.000 2 2012 2013
dbSNP: rs1182933
rs1182933
C12orf43
3 1.000 0.120 12 121016819 upstream gene variant C/T snv 0.26 0.700 1.000 2 2013 2014
dbSNP: rs2592902
rs2592902 		2 1.000 0.080 1 159685936 intergenic variant G/A;T snv 0.35 0.700 1.000 2 2016 2019
dbSNP: rs3093068
rs3093068 		3 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 0.800 1.000 2 2013 2018
dbSNP: rs10518765
rs10518765
UNC13C
3 1.000 0.040 15 54388434 intron variant A/C snv 0.16 0.700 1.000 1 2007 2007
dbSNP: rs112635299
rs112635299
SERPINA2
7 1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs12427353
rs12427353
HNF1A
2 1.000 0.080 12 120989098 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12960928
rs12960928 		2 1.000 0.080 18 60230570 intergenic variant T/C snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs1529711
rs1529711
CARM1
4 1.000 0.080 19 10912758 intron variant C/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs157595
rs157595 		3 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1582763
rs1582763
MS4A4A
2 1.000 0.080 11 60254475 intron variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs174574
rs174574
FADS2
7 1.000 0.080 11 61832870 intron variant A/C snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs17519972
rs17519972
GLMN ; RPAP2
2 1.000 0.080 1 92362948 intron variant A/C snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs1920792
rs1920792
HNF1A-AS1
2 1.000 0.080 12 120966781 intron variant T/C snv 0.43 0.700 1.000 1 2014 2014
dbSNP: rs2126259
rs2126259
LOC157273
9 1.000 8 9327636 intron variant T/C snv 0.87 0.700 1.000 1 2016 2016
dbSNP: rs2250417
rs2250417
BCO2
5 1.000 0.080 11 112214593 intron variant T/C snv 0.44 0.700 1.000 1 2014 2014
dbSNP: rs2287921
rs2287921
RASIP1
4 1.000 0.040 19 48725015 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2016 2016