"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC130000 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039901	NM_001387778.1(TPD52-MRPS28):c.435+12558CTACAGAAGGTGGAGCCC[6]	LOC130000644, MRPS28 +1 more	Microsatellite (intron variant)	MRPS28-related disorder	GLikely benign
Select item 3038476	NM_001387778.1(TPD52-MRPS28):c.435+12558CTACAGAAGGTGGAGCCC[3]	LOC130000644, MRPS28 +1 more	Microsatellite (intron variant)	MRPS28-related disorder	GLikely benign