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: rs267607167
rs267607167
1 1.000 1 160421171 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.800 1.000 1 2010 2010
dbSNP: rs267607168
rs267607168
1 1.000 1 160425122 missense variant T/C snv 0.800 1.000 1 2010 2010