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: rs1339756947
rs1339756947
1 1.000 0.080 17 21303189 missense variant C/A;T snv 2.0E-05 0.700 0
dbSNP: rs989026404
rs989026404
1 1.000 0.080 17 21304500 missense variant T/C;G snv 4.0E-06 0.700 0