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: rs767178508
rs767178508
5 0.851 0.120 13 20189143 missense variant C/T snv 1.2E-05 4.2E-05 0.010 1.000 1 2004 2004