List of variants in gene ROM1 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000327.4(ROM1):c.353G>C (p.Gly118Ala)	rs1799959	0.93846
NM_000327.4(ROM1):c.669G>C (p.Arg223=)	rs1801144	0.26271
NM_000327.3(ROM1):c.-329G>T	rs3923805	0.21125
NM_000327.4(ROM1):c.868del (p.Gln290fs)	rs548233813	0.00807
NM_000327.4(ROM1):c.686G>A (p.Arg229His)	rs150168119	0.00375
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.705C>T (p.Ala235=)	rs367735986	0.00048
NM_000327.4(ROM1):c.702C>T (p.Tyr234=)	rs138643139	0.00007
NM_000327.4(ROM1):c.353= (p.Gly118=)
NM_000327.4(ROM1):c.397C>T (p.Leu133=)	rs566866016

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