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: rs150633473
rs150633473
1 1.000 0.040 1 203499804 missense variant C/T snv 6.0E-05 7.7E-05 0.010 1.000 1 2002 2002