rs781366461, 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, Visceral, 5, Autosomal
CUI: C3495537
Disease: Heterotaxy, Visceral, 5, Autosomal
8 1.000 0.120 10 70435354 missense variant G/A snv 5.2E-05 0.700 1.000 2 1997 2009