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: rs1906953
rs1906953
4 0.882 0.040 6 34068669 intron variant C/T snv 0.25 0.820 1.000 3 2013 2016