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

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.451-9G>A	rs12313763	0.08467
NM_004985.5(KRAS):c.451-5565G>A	rs200970347	0.00031
NM_004985.5(KRAS):c.24A>G (p.Val8=)	rs147406419	0.00025
NM_004985.5(KRAS):c.264A>G (p.Lys88=)	rs370920665	0.00021
NM_004985.5(KRAS):c.451-5535A>C	rs201170656	0.00019
NM_004985.5(KRAS):c.198A>G (p.Ala66=)	rs200229810	0.00016
NM_004985.5(KRAS):c.451-14T>C	rs372508498	0.00014
NM_004985.5(KRAS):c.451-5560T>A	rs373169526	0.00006
NM_033360.4(KRAS):c.249C>T (p.Ala83=)	rs751117590	0.00002
NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del)	rs397517043

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