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
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 3 2016 2019
dbSNP: rs10935733
rs10935733
1 3 148905181 intron variant T/C snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs11096402
rs11096402
1 X 134693838 intron variant G/A snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs13266210
rs13266210
1 8 41675996 intron variant A/G snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs138715366
rs138715366
1 7 44206672 intron variant C/T snv 5.9E-03 0.700 1.000 2 2016 2019
dbSNP: rs1415701
rs1415701
3 6 130024690 intron variant G/A snv 0.31 0.700 1.000 2 2016 2019
dbSNP: rs2242116
rs2242116
1 3 46899626 intron variant A/G snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs2971669
rs2971669
GCK
1 7 44192179 intron variant C/T snv 0.30 0.700 1.000 2 2018 2019
dbSNP: rs35261542
rs35261542
3 1.000 0.080 6 20675561 intron variant C/A snv 0.26 0.700 1.000 2 2016 2019
dbSNP: rs6040076
rs6040076
1 20 10678234 intron variant G/A;C snv 0.700 1.000 2 2016 2019
dbSNP: rs9883204
rs9883204
1 3 123377973 intron variant T/A;C snv 0.800 1.000 2 2010 2013
dbSNP: rs10147938
rs10147938
1 14 31416745 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10173538
rs10173538
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10402712
rs10402712
1 19 33435107 intron variant G/A snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs10509669
rs10509669
1 10 94210156 intron variant A/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs10734564
rs10734564
1 11 48138877 intron variant A/G snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs10814916
rs10814916
7 0.851 0.200 9 4293150 intron variant A/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10872678
rs10872678
1 6 151718829 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10895278
rs10895278
1 11 102224604 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10913200
rs10913200
1 1 176552519 intron variant G/A snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs1101081
rs1101081
1 6 151711782 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs11051061
rs11051061
1 12 30761734 intron variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs11055034
rs11055034
2 1.000 0.080 12 12737692 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11082304
rs11082304
6 18 23141009 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11085720
rs11085720
1 19 10207087 intron variant A/G snv 0.54 0.700 1.000 1 2019 2019