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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.35G>A (p.Gly12Asp)	rs121913237	0.00001
NM_002524.5(NRAS):c.173C>T (p.Thr58Ile)	rs2101742052
NM_002524.5(NRAS):c.181C>A (p.Gln61Lys)	rs121913254
NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)	rs121434595
NM_002524.5(NRAS):c.38G>A (p.Gly13Asp)	rs121434596

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