List of variants in gene KRAS reported as likely benign by Clinical Genetics, Academic Medical Center

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.24A>G (p.Val8=)	rs147406419	0.00025
NM_004985.5(KRAS):c.451-5535A>C	rs201170656	0.00019
NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del)	rs397517043

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