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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GHRHR
(P18L)
Single nucleotide variant
(missense variant)
Isolated growth hormone deficiency type IB
+1 more
GUncertain significance
GHRHR
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GHRHR
Single nucleotide variant
(intron variant)
Isolated growth hormone deficiency type IB
+1 more
GConflicting classifications of pathogenicity
GH-LCR, GH1
(E67D +1 more)
Single nucleotide variant
(missense variant +1 more)
Isolated growth hormone deficiency type IB
+1 more
GUncertain significance
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