List of variants in gene KRAS reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.451-5622G>A	rs755877953	0.00003
NM_033360.4(KRAS):c.389C>T (p.Ala130Val)	rs730880473	0.00002
NM_004985.5(KRAS):c.112-12C>T	rs202104024	0.00001
NM_004985.5(KRAS):c.149C>T (p.Thr50Ile)	rs1407509439	0.00001
NM_004985.5(KRAS):c.451-5538A>G	rs755967833	0.00001
NM_033360.4(KRAS):c.*4+1G>A	rs780979221	0.00001
NM_033360.4(KRAS):c.491G>A (p.Arg164Gln)	rs758575947	0.00001
NM_004985.5(KRAS):c.179G>A (p.Gly60Asp)
NM_004985.5(KRAS):c.220A>C (p.Thr74Pro)	rs770020203
NM_004985.5(KRAS):c.291-10del	rs727503991
NM_033360.4(KRAS):c.140A>G (p.Asp47Gly)	rs1565885006
NM_033360.4(KRAS):c.291-5C>G	rs1565884303
NM_033360.4(KRAS):c.400G>A (p.Ala134Thr)	rs1565884227
NM_033360.4(KRAS):c.461A>T (p.Asp154Val)

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