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Links from MedGen

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZBTB7A
(G276R)
Single nucleotide variant
(missense variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GUncertain significance
ZBTB7A
(L33fs)
Deletion
(frameshift variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
ZBTB7A
(A226fs)
Duplication
(frameshift variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
ZBTB7A
(Q142*)
Single nucleotide variant
(nonsense)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GUncertain significance
ZBTB7A
(A175fs)
Duplication
(frameshift variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GLikely pathogenic
ZBTB7A
(D452N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
ZBTB7A
(N215fs)
Duplication
(frameshift variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
ZBTB7A
(Q370*)
Single nucleotide variant
(nonsense)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
ZBTB7A
(S56I)
Indel
(missense variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
ZBTB7A
(R530fs)
Deletion
(frameshift variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
ZBTB7A
(C384W)
Single nucleotide variant
(missense variant)
Macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin
GPathogenic
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