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: rs111033553
rs111033553
2 0.925 0.080 6 116120332 missense variant C/T snv 0.010 1.000 1 1998 1998