List of variants in gene KRAS reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 13

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HGVS	dbSNP	gnomAD frequency
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.198A>G (p.Ala66=)	rs200229810	0.00016
NM_004985.5(KRAS):c.451-14T>C	rs372508498	0.00014
NM_033360.4(KRAS):c.5-11A>G	rs369047577	0.00008
NM_004985.5(KRAS):c.451-5560T>A	rs373169526	0.00006
NM_004985.5(KRAS):c.451-5652C>T	rs727505314	0.00004
NM_004985.5(KRAS):c.451-5604T>A	rs397517476	0.00002
NM_004985.5(KRAS):c.33T>C (p.Ala11=)	rs397517039
NM_004985.5(KRAS):c.450+11C>G	rs727504633
NM_004985.5(KRAS):c.451-10T>C	rs876657481
NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del)	rs397517043

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