List of variants in gene combination LPAR6, RB1 reported as likely benign for not provided

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001162498.3(LPAR6):c.921G>T (p.Trp307Cys)	rs17071686	0.00841
NM_001162498.3(LPAR6):c.801A>C (p.Ala267=)	rs4151552	0.00148
NM_001162498.3(LPAR6):c.174C>T (p.Asn58=)	rs779556016	0.00005
NM_000321.3(RB1):c.1695+29942T>C
NM_000321.3(RB1):c.1695+30396A>G	rs2233573
NM_000321.3(RB1):c.1695+34353G>A
NM_001162498.3(LPAR6):c.132C>T (p.Cys44=)
NM_001162498.3(LPAR6):c.285G>C (p.Leu95=)
NM_001162498.3(LPAR6):c.370_375del (p.Ser124_Lys125del)
NM_001162498.3(LPAR6):c.456T>G (p.Val152=)
NM_001162498.3(LPAR6):c.540T>C (p.Tyr180=)

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