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: rs1799777
rs1799777
1 9 104903754 5 prime UTR variant -/C delins 0.10 0.700 1.000 1 2018 2018
dbSNP: rs55951234
rs55951234
2 22 38205423 5 prime UTR variant -/CTC delins 0.700 1.000 1 2018 2018
dbSNP: rs111524356
rs111524356
2 2 65057022 intron variant -/GTGGATGCAGCAG;TGGATGCAGCAG;TGGATGCGGCAG;TGTATGCAGCAG delins 0.45 0.700 1.000 1 2018 2018
dbSNP: rs142815467
rs142815467
3 19 46291277 intergenic variant -/T delins 0.12 0.700 1.000 1 2017 2017
dbSNP: rs4665710
rs4665710
6 2 20998163 downstream gene variant A/C snv 0.76 0.700 1.000 3 2015 2019
dbSNP: rs10861661
rs10861661
1 12 106780868 intron variant A/C snv 0.23 0.700 1.000 2 2017 2017
dbSNP: rs10152811
rs10152811
1 15 86311359 intron variant A/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs11216126
rs11216126
4 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs12158587
rs12158587
1 22 25623573 intron variant A/C snv 2.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs1351452
rs1351452
1 11 117072638 intron variant A/C snv 0.86 0.700 1.000 1 2009 2009
dbSNP: rs16991720
rs16991720
4 21 34484464 intron variant A/C snv 0.700 1.000 1 2012 2012
dbSNP: rs17058802
rs17058802
1 4 172722489 intron variant A/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs1884507
rs1884507
1 20 52395625 intron variant A/C snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs2227368
rs2227368
1 19 16896136 non coding transcript exon variant A/C snv 6.6E-03 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs236911
rs236911
1 11 117214554 non coding transcript exon variant A/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2740488
rs2740488
9 0.827 0.120 9 104899461 intron variant A/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs2820441
rs2820441
1 1 219561618 downstream gene variant A/C snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs2971672
rs2971672
GCK
4 7 44166307 intron variant A/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs2980853
rs2980853
16 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs34515106
rs34515106
2 2 68380846 missense variant A/C snv 6.7E-03 1.9E-03 0.700 1.000 1 2012 2012
dbSNP: rs3827216
rs3827216
APP
1 21 25924954 intron variant A/C snv 1.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs453789
rs453789
1 17 44118647 intron variant A/C snv 0.97 0.700 1.000 1 2012 2012
dbSNP: rs480392
rs480392
3 1 107436774 synonymous variant A/C snv 0.99 0.95 0.700 1.000 1 2012 2012
dbSNP: rs6726798
rs6726798
3 2 218436132 intron variant A/C snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs6872314
rs6872314
1 5 75440240 intron variant A/C snv 0.35 0.700 1.000 1 2009 2009