rs121909283, NODAL

N. diseases: 4
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 0.882 0.120 10 70435399 stop gained C/A;T snv 3.1E-04 0.800 1.000 2 1997 2009
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 0.882 0.120 10 70435399 stop gained C/A;T snv 3.1E-04 0.700 1.000 10 1993 2014
Heterotaxy Syndrome
CUI: C3178805
Disease: Heterotaxy Syndrome
8 0.882 0.120 10 70435399 stop gained C/A;T snv 3.1E-04 0.700 0
Wolff-Parkinson-White Syndrome
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
22 0.882 0.120 10 70435399 stop gained C/A;T snv 3.1E-04 0.700 0