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: rs1057519874
rs1057519874
4 0.807 0.120 7 6387261 missense variant C/A;T snv 0.710 1.000 1 2014 2016
dbSNP: rs1057519948
rs1057519948
4 0.851 0.120 7 6387262 missense variant C/T snv 0.700 1.000 1 2016 2016