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: rs138880920
rs138880920
1 1.000 0.040 9 104826957 missense variant C/G snv 3.3E-03 1.8E-03 0.010 1.000 1 2005 2005