List of variants in gene combination HRAS, LRRC56 reported as likely benign for eyelid disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.357C>T (p.Asp119=)	rs111352454	0.00121
NM_005343.4(HRAS):c.330C>T (p.Pro110=)	rs200747280	0.00011
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser)	rs397517144	0.00004
NM_005343.4(HRAS):c.291-6T>G	rs766909143

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