List of variants in gene combination LPAR6, RB1 reported as likely benign for nervous system cancer

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.1695+30162G>T	rs749894411	0.00001
NM_000321.3(RB1):c.1695+30611_1695+30612del	rs1177544722

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