List of variants in gene KRAS reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.451-5617=	rs4362222	0.99825
NM_004985.5(KRAS):c.519T>C (p.Asp173=)	rs1137282	0.19382
NM_033360.4(KRAS):c.450+92A>G	rs76433096	0.14824
NM_004985.5(KRAS):c.451-9G>A	rs12313763	0.07930
NM_004985.5(KRAS):c.291-162A>C	rs61762369	0.06157
NM_033360.4(KRAS):c.290+74T>G	rs115908336	0.01631
NM_033360.4(KRAS):c.290+97A>C	rs11836509
NM_033360.4(KRAS):c.290+97A>T	rs11836509

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