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: rs1395219766
rs1395219766
ADAMTSL2
1 1.000 9 133537464 missense variant G/C snv 0.700 1.000 2 2008 2011