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: rs766001707
rs766001707
6 0.851 0.200 14 92096772 missense variant C/T snv 0.010 1.000 1 2006 2006