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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KDM4B, LOC130063244
(Q542E +1 more)
Single nucleotide variant
(missense variant)
KDM4B-related disorder
GUncertain significance
KDM4B, LOC130063244
(P573S +1 more)
Single nucleotide variant
(missense variant)
KDM4B-related disorder
GUncertain significance
KDM4B, LOC130063244
(G576S +1 more)
Single nucleotide variant
(missense variant)
KDM4B-related disorder
GLikely benign
KDM4B, LOC130063244
(A578P +1 more)
Single nucleotide variant
(missense variant)
KDM4B-related disorder
+1 more
GLikely benign
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