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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HYLS1, PUS3
(R435* +1 more)
Single nucleotide variant
(nonsense +1 more)
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
GPathogenic
HYLS1, PUS3
(R159H)
Single nucleotide variant
(5 prime UTR variant +2 more)
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
+1 more
GUncertain significance
HYLS1, PUS3
(T6fs)
Microsatellite
(frameshift variant +1 more)
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
GLikely pathogenic
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