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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNMT3B
(A384T +4 more)
Single nucleotide variant
(missense variant)
Immunodeficiency-centromeric instability-facial anomalies syndrome 1
+2 more
GBenign
DNMT3B
Single nucleotide variant
(intron variant)
Immunodeficiency-centromeric instability-facial anomalies syndrome 1
+2 more
GBenign/Likely benign
DNMT3B
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
DNMT3B
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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