Variants in gene NRAS with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.225C>T (p.Gly75=)	rs142739534	0.00123
NM_002524.5(NRAS):c.360G>A (p.Leu120=)	rs143020946	0.00034
NM_002524.5(NRAS):c.112-8A>G	rs9724626	0.00025
NM_002524.5(NRAS):c.36T>G (p.Gly12=)	rs759764705	0.00006
NM_002524.5(NRAS):c.291-8G>A	rs376187980	0.00004
NM_002524.5(NRAS):c.159G>A (p.Leu53=)	rs114668710	0.00001
NM_002524.5(NRAS):c.112-24dup	rs780595451
NM_002524.5(NRAS):c.451-21_451-19del	rs754048062

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