List of variants in gene ROM1 reported as benign for retinitis pigmentosa

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000327.4(ROM1):c.669G>C (p.Arg223=)	rs1801144	0.26271
NM_000327.3(ROM1):c.-329G>T	rs3923805	0.21125
NM_000327.3(ROM1):c.-438G>A	rs576371643	0.00715
NM_000327.4(ROM1):c.812T>C (p.Met271Thr)	rs137950927	0.00178
NM_000327.4(ROM1):c.342C>T (p.Leu114=)	rs537377404	0.00049
NM_000327.4(ROM1):c.724C>T (p.Arg242Ter)	rs147065010	0.00011

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