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: rs121908418
rs121908418
1 1.000 0.080 11 134258589 missense variant T/C snv 6.8E-05 7.0E-05 0.800 1.000 3 2003 2006