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: rs10423928
rs10423928
12 0.807 0.200 19 45679046 intron variant T/A snv 0.19 0.800 1.000 1 2010 2010
dbSNP: rs10830963
rs10830963
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs12243326
rs12243326
5 0.925 0.160 10 113029056 intron variant T/C snv 0.27 0.800 1.000 1 2010 2010
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 1 2010 2010
dbSNP: rs13421358
rs13421358
1 2 43020088 regulatory region variant C/T snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs150112597
rs150112597
1 2 176189453 missense variant G/C;T snv 2.4E-03; 4.1E-06 0.700 1.000 1 2017 2017
dbSNP: rs17271305
rs17271305
1 15 62040781 intron variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs17271340
rs17271340
2 15 62055686 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs17681684
rs17681684
1 17 9889451 missense variant G/A;C snv 0.22; 4.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs17683011
rs17683011
3 1.000 0.120 22 32049959 missense variant A/G snv 4.8E-02 4.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs17683430
rs17683430
2 1.000 0.120 22 32091713 missense variant G/A snv 4.9E-02 4.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs1800437
rs1800437
13 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 0.700 1.000 1 2017 2017
dbSNP: rs201111080
rs201111080
1 1 176670971 missense variant G/T snv 1.9E-04 1.8E-04 0.700 1.000 1 2017 2017
dbSNP: rs2042608
rs2042608
2 15 61940181 intron variant C/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs2877716
rs2877716
4 3 123375604 intron variant T/C snv 0.76 0.800 1.000 1 2010 2010
dbSNP: rs28929474
rs28929474
37 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs2943641
rs2943641
18 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs3741151
rs3741151
1 11 73309801 missense variant G/A;C;T snv 8.1E-06; 8.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs4746822
rs4746822
2 10 69223185 non coding transcript exon variant C/T snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs5015480
rs5015480
9 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634
22 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs7102710
rs7102710
3 11 14244067 intron variant T/C snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs7330796
rs7330796
1 13 75324027 intron variant T/C snv 0.76 0.700 1.000 1 2014 2014
dbSNP: rs780094
rs780094
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs78714016
rs78714016
1 17 7078084 missense variant G/A;T snv 4.0E-03 0.700 1.000 1 2017 2017