List of variants in gene YME1L1 reported as benign for optic atrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_014263.4(YME1L1):c.1720-36G>C	rs2480718	0.99189
NM_014263.4(YME1L1):c.*45C>T	rs9833	0.85438
NM_014263.4(YME1L1):c.2008-7G>A	rs11015538	0.23338
NM_014263.4(YME1L1):c.691+16A>G	rs2275752	0.22144
NM_014263.4(YME1L1):c.39A>G (p.Thr13=)	rs11538750	0.07544
NM_014263.4(YME1L1):c.541-16T>C	rs2275751	0.00418

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