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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZFP57
(A457T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
ZFP57
(T491S +1 more)
Single nucleotide variant
(missense variant)
ZFP57-related disorder
+4 more
GConflicting classifications of pathogenicity
ZFP57
(A273P +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
ZFP57
(N198S +1 more)
Single nucleotide variant
(missense variant)
ZFP57-related disorder
+4 more
GBenign
ZFP57
(R187C +1 more)
Single nucleotide variant
(missense variant)
ZFP57-related disorder
+2 more
GBenign
ZFP57
(Y106H +1 more)
Single nucleotide variant
(missense variant)
ZFP57-related disorder
+4 more
GConflicting classifications of pathogenicity
ZFP57
(T159S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
ZFP57
(Q150* +1 more)
Single nucleotide variant
(nonsense)
ZFP57-related disorder
+1 more
GLikely pathogenic
ZFP57
Single nucleotide variant
(intron variant)
ZFP57-related disorder
+1 more
GConflicting classifications of pathogenicity
ZFP57
Single nucleotide variant
(synonymous variant)
ZFP57-related disorder
+1 more
GConflicting classifications of pathogenicity
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