List of variants reported as 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.3848+15T>C	rs2412617	0.99680
NM_133171.5(ELMO2):c.1980T>C (p.Asp660=)	rs2257495	0.98384
NM_005401.5(PTPN14):c.-26G>A	rs10864100	0.83031
NM_005401.5(PTPN14):c.2688+26C>T	rs3013451	0.82386
NM_005401.5(PTPN14):c.978A>G (p.Arg326=)	rs7550799	0.82382
NM_005401.5(PTPN14):c.3252A>G (p.Glu1084=)	rs1135352	0.81332
NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	rs1042522	0.62654
NM_032208.3(ANTXR1):c.1185+16C>A	rs6749826	0.45542
NM_005401.5(PTPN14):c.758+5T>G	rs11580603	0.37880
NM_005401.5(PTPN14):c.*26G>A	rs2291831	0.15689
NM_133171.5(ELMO2):c.963G>A (p.Arg321=)	rs41310805	0.01127
NM_133171.5(ELMO2):c.1134G>A (p.Leu378=)	rs8124302	0.00264
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
GRCh37/hg19 8q23.3(chr8:114378494-114450308)
NM_005401.5(PTPN14):c.929+24del	rs11322819

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