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: rs496300
rs496300
2 1.000 0.040 21 43359800 intron variant C/T snv 0.73 0.700 1.000 1 2010 2010