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: rs727563
rs727563
1 1.000 0.040 22 41471373 intron variant C/T snv 0.59 0.700 1.000 1 2015 2015