Related gene-specific medical variations for Gene (Select 54953) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302132	NM_017847.6(ODR4):c.1000+2119A>G	OCLM, ODR4	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2403140	NM_017847.6(ODR4):c.1000+2087G>A	OCLM, ODR4 (S29N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328260	NM_017847.6(ODR4):c.1000+2015C>T	OCLM, ODR4 (P5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305455	NM_017847.6(ODR4):c.1000+2014C>T	OCLM, ODR4 (P5S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302841	NM_017847.6(ODR4):c.1000+2075T>C	OCLM, ODR4 (I25T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212827	NM_017847.6(ODR4):c.1000+2056A>G	OCLM, ODR4 (I19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 715470	NM_017847.6(ODR4):c.1000+2105C>G	OCLM, ODR4	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar