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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIR4733HG, LOC111811965
+1 more
Single nucleotide variant
(5 prime UTR variant)
Neurofibromatosis-Noonan syndrome
+4 more
GUncertain significance
LOC111811965, MIR4733HG
+1 more
(R5S)
Single nucleotide variant
(missense variant)
Neurofibromatosis, type 1
+4 more
GUncertain significance
LOC111811965, MIR4733HG
+1 more
(P6L)
Single nucleotide variant
(missense variant)
Neurofibromatosis, familial spinal
+6 more
GUncertain significance
MIR4733HG, LOC111811965
+1 more
Single nucleotide variant
(intron variant)
Neurofibromatosis, familial spinal
+4 more
GLikely benign
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