List of variants in gene combination ARMS2, HTRA1 reported as likely benign for retinal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002775.5(HTRA1):c.102C>T (p.Ala34=)	rs1049331	0.22934
NM_002775.5(HTRA1):c.77G>A (p.Arg26Gln)	rs190036021	0.01411
NM_002775.5(HTRA1):c.-57C>A	rs554513888	0.01387
NM_001099667.3(ARMS2):c.298-14_298-13insG	rs529644268	0.01269
NM_002775.5(HTRA1):c.59C>T (p.Ala20Val)	rs369149111	0.00841
NM_001099667.3(ARMS2):c.298-4del	rs369018824
NM_002775.5(HTRA1):c.108G>C (p.Gly36=)	rs2293870
NM_002775.5(HTRA1):c.108G>T (p.Gly36=)	rs2293870

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