List of variants in gene KRAS reported as likely benign for not provided

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.451-9G>A	rs12313763	0.08467
NM_004985.5(KRAS):c.450+304T>A	rs1252899211	0.04067
NM_033360.4(KRAS):c.5-240G>A	rs61763587	0.01417
NM_004985.5(KRAS):c.450+296T>A	rs1362019931	0.01277
NM_004985.5(KRAS):c.-12+116G>T	rs61759619	0.01168
NM_033360.4(KRAS):c.291-311A>G	rs138809689	0.00663
NM_033360.4(KRAS):c.451-224T>A	rs145862422	0.00456
NM_004985.5(KRAS):c.291-128T>G	rs113376636	0.00419
NM_004985.5(KRAS):c.-11-324T>G	rs61759634	0.00399
NM_033360.4(KRAS):c.111+239A>G	rs187904655	0.00386
NM_033360.4(KRAS):c.*3766A>G	rs529959450	0.00108
NM_033360.4(KRAS):c.*1826C>G	rs539213224	0.00073
NM_004985.5(KRAS):c.451-5565G>A	rs200970347	0.00031
NM_004985.5(KRAS):c.24A>G (p.Val8=)	rs147406419	0.00025
NM_033360.4(KRAS):c.*4549G>C	rs545014897	0.00020
NM_004985.5(KRAS):c.451-5535A>C	rs201170656	0.00019
NM_033360.4(KRAS):c.5-11A>G	rs369047577	0.00008
NM_004985.5(KRAS):c.451-5560T>A	rs373169526	0.00006
NM_033360.4(KRAS):c.112-10C>T	rs760989619	0.00004
NM_033360.4(KRAS):c.93A>G (p.Glu31=)	rs377354475	0.00004
NM_004985.5(KRAS):c.451-5604T>A	rs397517476	0.00002
NM_004985.5(KRAS):c.411T>C (p.Tyr137=)	rs752731198	0.00001
NM_004985.5(KRAS):c.456T>G (p.Val152=)	rs767947451	0.00001
NM_033360.4(KRAS):c.-9C>T	rs370230526	0.00001
NM_033360.4(KRAS):c.450+13G>A	rs1057523949	0.00001
NM_004985.5(KRAS):c.*4059A>G
NM_004985.5(KRAS):c.451-5327G>A	rs114748473
NM_004985.5(KRAS):c.451-5604T>C	rs397517476
NM_004985.5(KRAS):c.453T>C (p.Gly151=)	rs2141481751
NM_004985.5(KRAS):c.528GAA[1] (p.Lys180del)	rs397517043
NM_033360.4(KRAS):c.*671C>T	rs566222739

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