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: rs121918498
rs121918498
2 1.000 0.080 10 121520162 missense variant CG/AA mnv 0.010 1.000 1 1997 1997