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: rs766578118
rs766578118
1 1.000 0.040 17 82830615 missense variant C/G;T snv 3.2E-05; 3.2E-05 0.010 1.000 1 2008 2008