List of variants in gene ACSF3 reported as benign for not specified

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001243279.3(ACSF3):c.51G>C (p.Ala17=)	rs7201122	0.91794
NM_001243279.3(ACSF3):c.5T>C (p.Leu2Pro)	rs7188200	0.72412
NM_001243279.3(ACSF3):c.354T>C (p.Ser118=)	rs6500528	0.72028
NM_001243279.3(ACSF3):c.342G>C (p.Ala114=)	rs6500527	0.72026
NM_001243279.3(ACSF3):c.315T>C (p.Asp105=)	rs7193255	0.71937
NM_001243279.3(ACSF3):c.369C>A (p.Val123=)	rs6500529	0.71928
NM_001243279.3(ACSF3):c.306C>T (p.Cys102=)	rs6500526	0.71888
NM_001243279.3(ACSF3):c.1347G>A (p.Leu449=)	rs12447947	0.24857
NM_001243279.3(ACSF3):c.854C>T (p.Pro285Leu)	rs143793502	0.09373
NM_001243279.3(ACSF3):c.49G>C (p.Ala17Pro)	rs11547019	0.03850
NM_001243279.3(ACSF3):c.667-12C>T	rs72817437	0.03381
NM_001243279.3(ACSF3):c.1367-13C>G	rs140859425	0.02493
NM_001243279.3(ACSF3):c.297C>T (p.Ser99=)	rs59213357	0.01079
NM_001243279.3(ACSF3):c.1367-6C>T	rs113343336	0.00901
NM_001243279.3(ACSF3):c.1134G>A (p.Val378=)	rs141088268	0.00369
NM_001243279.3(ACSF3):c.-193-14A>G	rs181386231	0.00139
NM_001243279.3(ACSF3):c.-14_-13insCCAGGAGGCTCCCGGGAGC	rs11273288

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