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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZC3H14
(R104Q +1 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal recessive 56
GUncertain significance
ZC3H14
(S130C +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
ZC3H14
(K223R +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal recessive 56
+1 more
GUncertain significance
ZC3H14
(P377L +2 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal recessive 56
GUncertain significance
ZC3H14
(N51S)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 56
GUncertain significance
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