C1837615[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031947	NM_001270974.2(HYDIN):c.15092C>T (p.Ser5031Leu)	HYDIN (S5031L)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 5	GUncertain significance
Select item 1031946	NM_001270974.2(HYDIN):c.14658+5G>A	HYDIN	Single nucleotide variant (intron variant)	Primary ciliary dyskinesia 5	GUncertain significance
Select item 1031945	NM_001270974.2(HYDIN):c.11638G>A (p.Asp3880Asn)	HYDIN (D3880N)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 5	GUncertain significance
Select item 1027858	NM_001270974.2(HYDIN):c.10247T>G (p.Val3416Gly)	HYDIN (V3416G)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 5	GUncertain significance
Select item 1031949	NM_001270974.2(HYDIN):c.9248+17C>G	HYDIN	Single nucleotide variant (intron variant)	Primary ciliary dyskinesia 5	GUncertain significance
Select item 1031948	NM_001270974.2(HYDIN):c.7483G>A (p.Asp2495Asn)	HYDIN (D2495N)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia 5	GUncertain significance
Select item 2441712	NM_001270974.2(HYDIN):c.3042+139A>G	HYDIN	Single nucleotide variant (3 prime UTR variant +1 more)	Primary ciliary dyskinesia 5	GUncertain significance

ClinVar