"YME1L1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043033	NM_014263.4(YME1L1):c.692-4C>T	YME1L1	Single nucleotide variant (intron variant)	YME1L1-related condition	GLikely benign
Select item 1986186	NM_014263.4(YME1L1):c.168+1417C>T	YME1L1	Single nucleotide variant (intron variant)	YME1L1-related condition +1 more	GConflicting classifications of pathogenicity
Select item 1225456	NM_014263.4(YME1L1):c.168+1269A>G	YME1L1 (N67S)	Single nucleotide variant (missense variant +1 more)	YME1L1-related condition +1 more	GBenign

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