C4310628[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1259033	NM_014263.4(YME1L1):c.*45C>T	YME1L1	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 1277257	NM_014263.4(YME1L1):c.2008-7G>A	YME1L1	Single nucleotide variant (intron variant)	Optic atrophy 11 +1 more	GBenign
Select item 1220690	NM_014263.4(YME1L1):c.1720-36G>C	YME1L1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1276244	NM_014263.4(YME1L1):c.691+16A>G	YME1L1	Single nucleotide variant (intron variant)	Optic atrophy 11 +1 more	GBenign
Select item 1278570	NM_014263.4(YME1L1):c.541-16T>C	YME1L1	Single nucleotide variant (intron variant)	Optic atrophy 11 +1 more	GBenign
Select item 1236887	NM_014263.4(YME1L1):c.39A>G (p.Thr13=)	YME1L1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar