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: rs121913516
rs121913516
KIT
3 1.000 0.071 4 54729353 missense variant C/T snp 4.0E-06 0.010 1.000 1 2005 2005