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: rs1553163562
rs1553163562
ROR1
1 1.000 1 64178248 missense variant G/C snv 0.700 1.000 1 2016 2016