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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NODAL
(G260R +1 more)
Single nucleotide variant
(missense variant)
Visceral heterotaxy
+4 more
GConflicting classifications of pathogenicity
NODAL
Single nucleotide variant
(synonymous variant)
Heterotaxy, visceral, 5, autosomal
+3 more
GBenign
NODAL
(H165R +1 more)
Single nucleotide variant
(missense variant)
NODAL-related condition
+4 more
GBenign
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