"FAM177A1-related disorder"[Disease/phenotype] AND "Undiagnosed Diseas - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 870589	NC_000014.9:g.35044389_35052476del	LOC130055485, FAM177A1 +3 more	Deletion (genic upstream transcript variant)	FAM177A1-related disorder	GLikely pathogenic
Select item 870577	NC_000014.9:g.35077780_35087566del	FAM177A1, LOC101927178 +1 more	Deletion	FAM177A1-related disorder	GLikely pathogenic