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: rs149151043
rs149151043
1 1.000 0.120 16 2103617 missense variant C/T snv 6.1E-03 6.3E-03 0.700 1.000 20 1996 2009