List of variants in gene combination HRAS, LRRC56 reported as pathogenic by GeneDx

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.179G>A (p.Gly60Asp)	rs730880460
NM_005343.4(HRAS):c.179G>T (p.Gly60Val)	rs730880460
NM_005343.4(HRAS):c.181C>A (p.Gln61Lys)	rs28933406
NM_005343.4(HRAS):c.187G>A (p.Glu63Lys)	rs121917756
NM_005343.4(HRAS):c.34G>A (p.Gly12Ser)	rs104894229
NM_005343.4(HRAS):c.34G>T (p.Gly12Cys)	rs104894229
NM_005343.4(HRAS):c.350A>G (p.Lys117Arg)	rs104894227
NM_005343.4(HRAS):c.35G>A (p.Gly12Asp)	rs104894230
NM_005343.4(HRAS):c.35G>C (p.Gly12Ala)	rs104894230
NM_005343.4(HRAS):c.35G>T (p.Gly12Val)	rs104894230
NM_005343.4(HRAS):c.35_36delinsAA (p.Gly12Glu)	rs727503094
NM_005343.4(HRAS):c.35_36delinsAT (p.Gly12Asp)	rs727503094
NM_005343.4(HRAS):c.35_36delinsCT (p.Gly12Ala)	rs727503094
NM_005343.4(HRAS):c.35_36delinsTA (p.Gly12Val)	rs727503094
NM_005343.4(HRAS):c.35_36delinsTT (p.Gly12Val)	rs727503094
NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)	rs104894228
NM_005343.4(HRAS):c.38G>A (p.Gly13Asp)	rs104894226
NM_005343.4(HRAS):c.38G>T (p.Gly13Val)	rs104894226
NM_005343.4(HRAS):c.468C>G (p.Phe156Leu)	rs770648642

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