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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FZD2
(Y287H)
Single nucleotide variant
(missense variant)
Autosomal dominant omodysplasia
GUncertain significance
FZD2
(S547L)
Single nucleotide variant
(missense variant)
Autosomal dominant omodysplasia
GUncertain significance
FZD2
(L136Q)
Single nucleotide variant
(missense variant)
Autosomal dominant omodysplasia
GUncertain significance
FZD2
(E134Q)
Single nucleotide variant
(missense variant)
Autosomal dominant omodysplasia
GUncertain significance
FZD2
(W548*)
Single nucleotide variant
not provided
+2 more
GPathogenic
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