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: rs368625677
rs368625677
1 1.000 0.160 19 49637121 missense variant C/G;T snv 4.1E-06; 3.3E-05 0.010 1.000 1 2014 2014