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: rs770564395
rs770564395
1 1.000 0.040 22 41784745 missense variant C/G;T snv 4.1E-06; 4.1E-06 0.010 1.000 1 2018 2018