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: rs114499642
rs114499642
1 13 103976035 intergenic variant C/G snv 1.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs17108533
rs17108533
1 14 70783085 intron variant C/A;G;T snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs17126180
rs17126180
1 12 51870172 intergenic variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17689437
rs17689437
1 16 68566448 3 prime UTR variant C/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs17706989
rs17706989
1 16 78536060 intron variant C/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs2142694
rs2142694
1 22 42146869 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2286720
rs2286720
1 3 42406979 synonymous variant G/A snv 0.10 7.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs2833556
rs2833556
1 21 31912988 intron variant G/A snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs3753242
rs3753242
1 1 2138242 intron variant C/T snv 7.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs4611189
rs4611189
1 11 40816163 intron variant G/A snv 3.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs74412765
rs74412765
1 14 34053698 intron variant C/T snv 5.9E-03 0.700 1.000 1 2018 2018
dbSNP: rs76872642
rs76872642
1 7 18629780 intron variant G/A snv 5.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs9771228
rs9771228
3 7 32282884 intron variant T/C snv 0.39 0.700 1.000 1 2016 2016