Source: ALL
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: rs1352947
rs1352947
KITLG
1 1.000 0.120 12 88566950 intron variant C/G;T snv 0.700 1.000 2 2009 2011