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: rs10893844
rs10893844 		2 11 128315955 regulatory region variant G/C snv 0.36 0.700 1.000 2 2016 2019