rs781389750, TCN2

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Congenital omphalocele
CUI: C0795690
Disease: Congenital omphalocele
13 1.000 0.080 22 30610913 missense variant A/G snv 4.0E-06 0.010 1.000 1 2012 2012