Related gene-specific medical variations for Gene (Select 113839546) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 913580	NM_012144.4(DNAI1):c.-116T>C	DNAI1, LOC113839546	Single nucleotide variant (5 prime UTR variant)	Kartagener syndrome	GLikely benign
Select item 366682	NM_012144.4(DNAI1):c.-83G>C	DNAI1, LOC113839546	Single nucleotide variant (5 prime UTR variant)	Kartagener syndrome	GUncertain significance
Select item 366681	NM_012144.4(DNAI1):c.-145C>T	DNAI1, LOC113839546	Single nucleotide variant (5 prime UTR variant)	Kartagener syndrome	GUncertain significance
Select item 366680	NM_012144.4(DNAI1):c.-170T>A	DNAI1, LOC113839546	Single nucleotide variant (5 prime UTR variant)	Primary ciliary dyskinesia	GUncertain significance
Select item 366679	NM_012144.4(DNAI1):c.-178G>C	DNAI1, LOC113839546	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GLikely benign
Select item 366678	NM_012144.4(DNAI1):c.-180G>A	DNAI1, LOC113839546	Single nucleotide variant (5 prime UTR variant)	Kartagener syndrome	GUncertain significance

ClinVar