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: rs1568018697
rs1568018697
2 17 82032437 missense variant C/T snv 0.700 0
dbSNP: rs1568018920
rs1568018920
2 17 82032785 missense variant A/T snv 0.700 0