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: rs137854532
rs137854532
4 0.882 0.160 20 58905443 missense variant C/T snv 0.010 1.000 1 2008 2008