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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZIC2
(M57I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ZIC2
Microsatellite
(inframe_insertion)
not specified
+2 more
GBenign/Likely benign
ZIC2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
ZIC2
Single nucleotide variant
(synonymous variant)
Holoprosencephaly 5
+2 more
GBenign
LOC110008580, ZIC2
Deletion
(inframe_deletion)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
ZIC2
Deletion
(inframe_deletion)
not provided
GUncertain significance
ZIC2
Single nucleotide variant
(synonymous variant)
not specified
GBenign
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