List of variants in gene ARMS2 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001099667.3(ARMS2):c.*376T>C	rs2672602	0.11668
NM_001099667.3(ARMS2):c.*385A>C	rs2672603	0.11652
NM_001099667.3(ARMS2):c.*373T>G	rs4752698	0.09758
NM_001099667.3(ARMS2):c.*45T>G	rs150019974	0.00424
NM_001099667.3(ARMS2):c.*161C>T	rs536799180	0.00078
NM_001099667.3(ARMS2):c.*204C>A	rs79134213	0.00063
NM_001099667.3(ARMS2):c.*107T>G	rs183542198	0.00025
NM_001099667.3(ARMS2):c.-9G>A	rs186211237	0.00007
NM_001099667.3(ARMS2):c.298-13A>G	rs7088128
NM_001099667.3(ARMS2):c.298-13A>T	rs7088128

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