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: rs121918666
rs121918666
3 0.882 0.160 5 1266524 missense variant C/T snv 8.2E-06 7.0E-06 0.800 1.000 5 2005 2012