Related gene-specific medical variations for Gene (Select 55567) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3083958	NM_017539.2(DNAH3):c.79A>T (p.Arg27Trp)	DNAH3, LDAF1 (R27W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083932	NM_017539.2(DNAH3):c.56C>G (p.Pro19Arg)	DNAH3, LDAF1 (P19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209843	NM_017539.2(DNAH3):c.68G>T (p.Arg23Leu)	DNAH3, LDAF1 (R23L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206001	NM_017539.2(DNAH3):c.102A>T (p.Glu34Asp)	DNAH3, LDAF1 (E34D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 688181	GRCh37/hg19 16p12.3(chr16:21023142-21159090)x1	DNAH3	Copy number loss	not provided	GUncertain significance
Select item 161706	NM_001347886.2(DNAH3):c.6130C>A (p.His2044Asn)	DNAH3 (H2090N +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

ClinVar