"PreventionGenetics, part of Exact Sciences"[submitter] AND "HMOX1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2632902	NM_002133.3(HMOX1):c.17C>A (p.Pro6His)	HMOX1 (P6H)	Single nucleotide variant (missense variant)	HMOX1-related disorder	GUncertain significance
Select item 1595809	NM_002133.3(HMOX1):c.135C>T (p.Asp45=)	HMOX1	Single nucleotide variant (synonymous variant)	HMOX1-related disorder +1 more	GLikely benign
Select item 1352914	NM_002133.3(HMOX1):c.253C>T (p.Arg85Cys)	HMOX1 (R85C)	Single nucleotide variant (missense variant)	HMOX1-related disorder +1 more	GUncertain significance
Select item 1165490	NM_002133.3(HMOX1):c.579C>T (p.Pro193=)	HMOX1	Single nucleotide variant (synonymous variant)	HMOX1-related disorder +1 more	GBenign
Select item 775454	NM_002133.3(HMOX1):c.603A>G (p.Glu201=)	HMOX1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1164758	NM_002133.3(HMOX1):c.676A>G (p.Lys226Glu)	HMOX1 (K226E)	Single nucleotide variant (missense variant)	HMOX1-related disorder +1 more	GBenign/Likely benign
Select item 1046119	NM_002133.3(HMOX1):c.709C>G (p.Arg237Gly)	HMOX1 (R237G)	Single nucleotide variant (missense variant)	HMOX1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1574282	NM_002133.3(HMOX1):c.741T>C (p.Ser247=)	HMOX1	Single nucleotide variant (synonymous variant)	HMOX1-related disorder +1 more	GLikely benign

ClinVar