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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPH2
(Q15E +1 more)
Single nucleotide variant
(nonsense +2 more)
Developmental delay with short stature, dysmorphic facial features, and sparse hair 2
GLikely pathogenic
DPH2
(L4P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
DPH2
(G10S +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DPH2
(E27* +2 more)
Single nucleotide variant
(missense variant +2 more)
Global developmental delay
+2 more
GUncertain significance
DPH2
(V90L +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DPH2
(V90M +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
DPH2
(V14L +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DPH2
(V16M +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
DPH2
(R125H +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
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