List of variants in gene combination HRAS, LRRC56 reported as benign for RASopathy

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.81T>C (p.His27=)	rs12628	0.34645
NM_005343.4(HRAS):c.477G>A (p.Leu159=)	rs140060409	0.00222
NM_005343.4(HRAS):c.357C>T (p.Asp119=)	rs111352454	0.00121
NM_005343.4(HRAS):c.257A>C (p.Asn86Thr)	rs138272051	0.00019
NM_005343.4(HRAS):c.369C>T (p.Arg123=)	rs200945755	0.00006
NM_005343.4(HRAS):c.309G>A (p.Val103=)	rs575789207	0.00004
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser)	rs397517144	0.00004
NM_005343.4(HRAS):c.378A>G (p.Glu126=)	rs397517140	0.00001
NM_005343.4(HRAS):c.291-6T>G	rs766909143
NM_176795.5(HRAS):c.488_507del (p.Leu163fs)	rs776060230

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