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: rs387907281
rs387907281
13 0.752 0.280 19 41970284 missense variant C/T snv 0.020 1.000 2 2017 2018
dbSNP: rs1064797245
rs1064797245
12 0.776 0.280 19 41970540 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs557052809
rs557052809
5 0.827 0.160 19 41975629 missense variant C/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs80356537
rs80356537
17 0.752 0.320 19 41970405 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015