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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AFG2A
(M1L)
Single nucleotide variant
(missense variant +1 more)
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
+2 more
GConflicting classifications of pathogenicity
AFG2A
(D628G +1 more)
Single nucleotide variant
(missense variant)
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
+1 more
GPathogenic/Likely pathogenic