"GRXCR1-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1297902	NM_001080476.3(GRXCR1):c.190G>A (p.Gly64Ser)	GRXCR1 (G64S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 178379	NM_001080476.3(GRXCR1):c.272G>T (p.Gly91Val)	GRXCR1 (G91V)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 987829	NM_001080476.3(GRXCR1):c.469G>T (p.Glu157Ter)	GRXCR1 (E157*)	Single nucleotide variant (nonsense)	GRXCR1-related disorder +2 more	GPathogenic/Likely pathogenic
Select item 3030880	NM_001080476.3(GRXCR1):c.477T>A (p.Val159=)	GRXCR1	Single nucleotide variant (synonymous variant)	GRXCR1-related disorder	GLikely benign
Select item 1585928	NM_001080476.3(GRXCR1):c.594C>T (p.Leu198=)	GRXCR1	Single nucleotide variant (synonymous variant)	GRXCR1-related disorder +1 more	GLikely benign
Select item 228734	NM_001080476.3(GRXCR1):c.785G>A (p.Arg262Gln)	GRXCR1 (R262Q)	Single nucleotide variant (missense variant)	GRXCR1-related disorder +3 more	GConflicting classifications of pathogenicity

ClinVar