List of variants in gene combination KRAS, LOC130007561 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.-48G>A	rs532564755	0.00168
NM_004985.5(KRAS):c.-122C>T	rs61759617	0.00137
NM_004985.5(KRAS):c.-160A>G	rs727503111	0.00124
NM_033360.4(KRAS):c.-48_-29dup	rs730880342	0.00063
NM_004985.5(KRAS):c.-27C>T	rs587781013	0.00015
NM_004985.5(KRAS):c.-163AGC[3]	rs397517034
NM_004985.5(KRAS):c.-167A>G	rs527326817
NM_004985.5(KRAS):c.-54C>T	rs397517036

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