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: rs1057519547
rs1057519547
2 0.925 0.040 5 45396550 missense variant C/T snv 0.700 0
dbSNP: rs1057519548
rs1057519548
2 0.925 0.040 5 45645575 missense variant C/G snv 0.700 0