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: rs747885829
rs747885829
1 1.000 0.040 1 247423957 missense variant C/T snv 2.0E-05 1.4E-05 0.010 1.000 1 2001 2001