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: rs144983062
rs144983062
2 1.000 0.080 12 55693209 missense variant C/T snv 4.3E-03 3.4E-03 0.010 1.000 1 2013 2013