List of variants in gene ARMS2 reported as uncertain significance for retinal disorder

Minimum submission review status:		Collection method:
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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_001099667.3(ARMS2):c.*251T>C	rs578150200	0.00136
NM_001099667.3(ARMS2):c.39G>A (p.Ala13=)	rs200123144	0.00028
NM_001099667.3(ARMS2):c.*15A>G	rs886046771	0.00006
NM_001099667.3(ARMS2):c.*313G>C	rs1237612173	0.00001
NM_001099667.3(ARMS2):c.23C>T (p.Pro8Leu)	rs778271975	0.00001
NM_001099667.3(ARMS2):c.*377dup	rs886046772
NM_001099667.3(ARMS2):c.*399A>G	rs2097478012
NM_001099667.3(ARMS2):c.-60G>T	rs886046769

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