List of variants in gene NODAL reported as benign for congenital anomaly of cardiovascular system

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_018055.5(NODAL):c.494A>G (p.His165Arg)	rs1904589	0.56006
NM_018055.5(NODAL):c.*740T>C	rs2279253	0.45837
NM_018055.5(NODAL):c.*722G>C	rs2279254	0.43411
NM_018055.5(NODAL):c.193+12C>T	rs10999338	0.35409
NM_018055.5(NODAL):c.*479C>T	rs80138796	0.01102
NM_018055.5(NODAL):c.*886G>A	rs58468830	0.01100
NM_018055.5(NODAL):c.*404T>C	rs77232076	0.01099
NM_018055.5(NODAL):c.*62A>T	rs76889088	0.01097
NM_018055.5(NODAL):c.588C>G (p.Leu196=)	rs2231959	0.00714
NM_018055.5(NODAL):c.216C>T (p.Asn72=)	rs138195571	0.00124
NM_018055.5(NODAL):c.357C>T (p.Pro119=)	rs77151171	0.00038
NM_018055.5(NODAL):c.548G>A (p.Arg183Gln)	rs104894169	0.00023
NM_018055.5(NODAL):c.607G>A (p.Glu203Lys)	rs10999334	0.00015
NM_018055.5(NODAL):c.816C>T (p.Asn272=)	rs774058854	0.00007
NM_018055.5(NODAL):c.*356G>A	rs556853359

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