"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC129935 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3054076	NM_014905.5(GLS):c.-212GCA[24]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3054034	NM_014905.5(GLS):c.-212GCA[23]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3047419	NM_014905.5(GLS):c.-212GCA[19]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3030444	NM_014905.5(GLS):c.-212GCA[26]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3054764	NM_014905.5(GLS):c.-212GCA[11]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3047867	NM_014905.5(GLS):c.-212GCA[12]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3047628	NM_014905.5(GLS):c.-212GCA[13]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3032445	NM_014905.5(GLS):c.-212GCA[9]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign
Select item 3031213	NM_014905.5(GLS):c.-212GCA[6]	GLS, LOC129935268	Microsatellite (5 prime UTR variant)	GLS-related disorder	GLikely benign

ClinVar