List of variants in gene RHO reported as likely benign for inborn disorder of amino acid metabolism

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000539.3(RHO):c.360C>T (p.Gly120=)	rs79765751	0.00312
NM_000539.3(RHO):c.152G>C (p.Gly51Ala)	rs149079952	0.00296
NM_000539.3(RHO):c.480C>A (p.Thr160=)	rs151063543	0.00180
NM_000539.3(RHO):c.*205C>T	rs202215179	0.00170
NM_000539.3(RHO):c.*467A>G	rs148165044	0.00161
NM_000539.3(RHO):c.381C>G (p.Ser127=)	rs146311684	0.00144
NM_000539.3(RHO):c.969C>T (p.Cys323=)	rs142771862	0.00075
NM_000539.3(RHO):c.*1200T>C	rs538744995	0.00051
NM_000539.3(RHO):c.891C>T (p.Ser297=)	rs142285818	0.00041
NM_000539.3(RHO):c.519C>T (p.Ala173=)	rs149722668	0.00029
NM_000539.3(RHO):c.624C>T (p.Phe208=)	rs113751838	0.00014
NM_000539.3(RHO):c.959C>A (p.Thr320Asn)	rs138831590	0.00011

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