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: rs370930012
rs370930012
1 1.000 1 103550999 missense variant C/A snv 2.8E-05 0.700 1.000 2 2014 2018