List of variants in gene ENO3 reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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_053013.4(ENO3):c.212A>G (p.Asn71Ser)	rs238238	0.65415
NM_053013.4(ENO3):c.254T>C (p.Val85Ala)	rs238239	0.43006
NM_053013.4(ENO3):c.1236-17C>T	rs77614413	0.02756
NM_053013.4(ENO3):c.240+17G>A	rs75279666	0.02755
NM_053013.4(ENO3):c.993C>T (p.Ala331=)	rs2230257	0.01604
NM_053013.4(ENO3):c.994G>A (p.Val332Ile)	rs61735456	0.00983
NM_053013.4(ENO3):c.1041C>T (p.Ile347=)	rs114208569	0.00794
NM_053013.4(ENO3):c.86-3del	rs151153333

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