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: rs1440032367
rs1440032367
COL11A2
3 0.925 0.080 6 33189169 missense variant G/C snv 7.0E-06 0.010 1.000 1 2007 2007