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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129997051, RSPH4A
Single nucleotide variant
(5 prime UTR variant)
Primary ciliary dyskinesia 11
GUncertain significance
LOC129997051, RSPH4A
Single nucleotide variant
(5 prime UTR variant)
Primary ciliary dyskinesia 11
GUncertain significance
RSPH4A, LOC129997051
Indel
(5 prime UTR variant)
not specified
+1 more
GConflicting classifications of pathogenicity
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