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: rs10902073
rs10902073 		1 11 1060934 TF binding site variant C/A snv 0.31 0.700 1.000 1 2013 2013