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: rs786201838
rs786201838
24 0.683 0.440 17 7674953 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs863224451
rs863224451
20 0.701 0.440 17 7673796 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876658468
rs876658468
24 0.689 0.440 17 7674954 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876659675
rs876659675
8 0.807 0.280 17 7674199 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs942158624
rs942158624
19 0.724 0.320 17 7674948 missense variant T/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1064796681
rs1064796681
1 1.000 0.120 17 7675091 missense variant C/T snv 0.010 < 0.001 1 2007 2007
dbSNP: rs876660821
rs876660821
22 0.689 0.400 17 7675075 missense variant A/C;G;T snv 0.010 < 0.001 1 1994 1994