List of variants in gene combination HRAS, LRRC56 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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_005343.4(HRAS):c.111+15G>A	rs41258054	0.04363
NM_005343.4(HRAS):c.257A>C (p.Asn86Thr)	rs138272051	0.00019
NM_005343.4(HRAS):c.330C>T (p.Pro110=)	rs200747280	0.00011
NM_005343.4(HRAS):c.369C>T (p.Arg123=)	rs200945755	0.00006
NM_005343.4(HRAS):c.222C>T (p.Thr74=)	rs372223975	0.00005
NM_005343.4(HRAS):c.36C>T (p.Gly12=)	rs727504424	0.00004
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser)	rs397517144	0.00004
NM_005343.4(HRAS):c.54G>A (p.Ala18=)	rs148380285	0.00003
NM_005343.4(HRAS):c.378A>G (p.Glu126=)	rs397517140	0.00001
NM_005343.4(HRAS):c.510G>A (p.Lys170=)	rs397517143	0.00001
NM_005343.4(HRAS):c.291-6T>G	rs766909143

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