Related gene-specific medical variations for Gene (Select 83693) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1301511	NC_000016.10:g.84145122G>C	DNAAF1, HSDL1 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1283046	NC_000016.10:g.84145087C>G	DNAAF1, HSDL1 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1279566	NC_000016.10:g.84145042A>G	DNAAF1, HSDL1 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign

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