List of variants reported as likely benign for cardiovascular organ benign neoplasm

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002253.4(KDR):c.1444T>C (p.Cys482Arg)	rs34231037	0.02299
NM_000546.6(TP53):c.97-6C>T	rs35117667	0.00847
NM_032208.3(ANTXR1):c.1553C>T (p.Ala518Val)	rs139807657	0.00253
NM_033360.4(KRAS):c.5-18A>G	rs200189105	0.00100
NM_000546.5(TP53):c.319T>C (p.Tyr107His)	rs368771578	0.00028
NM_004985.5(KRAS):c.24A>G (p.Val8=)	rs147406419	0.00025
NM_000546.6(TP53):c.672+18G>C	rs199578278	0.00014
NM_033360.4(KRAS):c.90C>T (p.Asp30=)	rs113623140	0.00011
NM_000546.6(TP53):c.847C>T (p.Arg283Cys)	rs149633775	0.00009
NM_033360.4(KRAS):c.4+5G>A	rs201789109	0.00006
NM_004985.5(KRAS):c.451-5652C>T	rs727505314	0.00004
NM_000546.6(TP53):c.-12C>T	rs375229869	0.00002
NM_133171.5(ELMO2):c.1416+9C>G	rs770529533	0.00002
NM_004985.5(KRAS):c.112-9C>T	rs727504298
NM_133171.5(ELMO2):c.1279+19del	rs76979752

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