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: rs1232620504
rs1232620504
1 1.000 0.120 6 31354503 missense variant C/T snv 0.010 < 0.001 1 2006 2006