List of variants in gene KRAS reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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.451-5538A>G	rs755967833	0.00001
NM_004985.5(KRAS):c.451-5604T>C	rs397517476
NM_004985.5(KRAS):c.508A>T (p.Met170Leu)	rs369501492

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