"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC129937 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3047604	NM_153240.4(NPHP3):c.-97_-70dup28	LOC129937587, NPHP3 +2 more	Microsatellite	NPHP3-related disorder	GLikely benign
Select item 343395	NM_153240.4(NPHP3):c.-69A>G	LOC129937587, NPHP3 +2 more	Single nucleotide variant (non-coding transcript variant)	not provided +4 more	GBenign