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: rs695646
rs695646
RASL10A
1 22 29313675 3 prime UTR variant C/-;CC;CCC delins 0.700 1.000 1 2016 2016