List of variants in gene ETV5 reported as 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004454.3(ETV5):c.970+241A>G	rs4686727	0.99417
NM_004454.3(ETV5):c.-74-273A>G	rs1516725	0.86299
NM_004454.3(ETV5):c.1312-62C>T	rs79060173	0.14650
NM_004454.3(ETV5):c.363-132G>A	rs77805826	0.12436
NM_004454.3(ETV5):c.-74-211G>A	rs12631658	0.07239
NM_004454.3(ETV5):c.1209+51G>T	rs59852126	0.06170
NM_004454.3(ETV5):c.362+107T>C	rs113586704	0.04249
NM_004454.3(ETV5):c.1210-176C>A	rs74607992	0.03547
NM_004454.3(ETV5):c.-74-242A>G	rs4686731	0.02349
NM_004454.3(ETV5):c.445C>G (p.Leu149Val)	rs78506201	0.01316
NM_004454.3(ETV5):c.1395G>A (p.Pro465=)	rs116699819	0.00803
NM_004454.3(ETV5):c.1399C>T (p.Leu467=)	rs115703632	0.00803
NM_004454.3(ETV5):c.1446G>A (p.Pro482=)	rs116523688	0.00395

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