List of variants in gene combination HRAS, LRRC56 reported as uncertain significance for benign neoplasm

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.506G>A (p.Arg169Gln)	rs142218590	0.00007
NM_005343.4(HRAS):c.508A>T (p.Lys170Ter)	rs372936166	0.00005
NM_005343.4(HRAS):c.505C>T (p.Arg169Trp)	rs151229168	0.00003
NM_005343.4(HRAS):c.11A>G (p.Tyr4Cys)	rs764622691	0.00001
NM_005343.4(HRAS):c.410A>C (p.Tyr137Ser)	rs1180561549	0.00001
NM_005343.4(HRAS):c.278T>C (p.Ile93Thr)	rs2133989896
NM_005343.4(HRAS):c.481C>T (p.Arg161Cys)	rs758956556
NM_005343.4(HRAS):c.491G>C (p.Arg164Pro)	rs753977266

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