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: rs1064793880
rs1064793880
ELN
1 1.000 0.080 7 74046755 missense variant C/T snv 0.010 1.000 1 2009 2009