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: rs12266458
rs12266458
1 1.000 0.080 10 49639951 intron variant C/T snv 0.11 0.010 1.000 1 2010 2010