rs555563029, NODAL

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.
Heterotaxy Syndrome
CUI: C3178805
Disease: Heterotaxy Syndrome
8 1.000 0.120 10 70435353 missense variant C/T snv 4.0E-06 0.700 0