List of variants in gene FLVCR2 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017791.3(FLVCR2):c.*187T>C	rs75002047	0.01000
NM_017791.3(FLVCR2):c.*1517T>C	rs114442666	0.00113
NM_017791.3(FLVCR2):c.905C>A (p.Ala302Asp)	rs183200579	0.00019
NM_017791.3(FLVCR2):c.727C>T (p.Arg243Trp)	rs146668840	0.00011
NM_017791.3(FLVCR2):c.*1319C>T	rs541678412	0.00003

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