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Links from OMIM

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CORIN
(K317E +1 more)
Single nucleotide variant
(missense variant)
Preeclampsia/eclampsia 5
GPathogenic
GATA6
(S184N)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
NKX2-5
(P59A)
Single nucleotide variant
(missense variant)
Ventricular septal defect 3
GPathogenic
GATA4
(R43W)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
GUncertain significance
GATA4
(G296R +2 more)
Single nucleotide variant
(missense variant +1 more)
Ventricular septal defect 1
GPathogenic
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