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: rs5751902
rs5751902
2 1.000 0.080 22 24600663 intron variant C/T snv 0.29 0.700 1.000 1 2011 2011