Variants in gene KRAS with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.451-5535A>C	rs201170656	0.00019
NM_033360.4(KRAS):c.93A>G (p.Glu31=)	rs377354475	0.00004
NM_033360.4(KRAS):c.249C>T (p.Ala83=)	rs751117590	0.00002
NM_004985.5(KRAS):c.291-10del	rs727503991
NM_004985.5(KRAS):c.451-5604T>C	rs397517476

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