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: rs1557507208
rs1557507208
1 1.000 1 58667102 missense variant T/C snv 0.700 0
dbSNP: rs1557518298
rs1557518298
1 1.000 1 58681876 stop gained C/A snv 0.700 0