"PreventionGenetics, part of Exact Sciences"[submitter] AND "GLRA2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3037510	NM_002063.4(GLRA2):c.249A>G (p.Gly83=)	GLRA2	Single nucleotide variant (synonymous variant +2 more)	GLRA2-related disorder	GUncertain significance
Select item 3039889	NM_002063.4(GLRA2):c.324G>A (p.Ala108=)	GLRA2	Single nucleotide variant (synonymous variant)	GLRA2-related disorder	GLikely benign
Select item 3054739	NM_002063.4(GLRA2):c.931-18TC[10]	FANCB, GLRA2	Microsatellite (intron variant)	GLRA2-related disorder	GLikely benign
Select item 3047336	NM_002063.4(GLRA2):c.1074G>A (p.Gln358=)	FANCB, GLRA2	Single nucleotide variant (synonymous variant)	GLRA2-related disorder	GLikely benign
Select item 780683	NM_002063.4(GLRA2):c.1089C>T (p.Asp363=)	FANCB, GLRA2	Single nucleotide variant (synonymous variant)	GLRA2-related disorder +1 more	GBenign
Select item 3051531	NM_002063.4(GLRA2):c.1128G>A (p.Gly376=)	FANCB, GLRA2	Single nucleotide variant (synonymous variant)	GLRA2-related disorder	GLikely benign
Select item 3046679	NM_002063.4(GLRA2):c.1172C>T (p.Ala391Val)	FANCB, GLRA2 (A302V +1 more)	Single nucleotide variant (missense variant)	GLRA2-related disorder	GLikely benign
Select item 2635551	NM_002063.4(GLRA2):c.1221C>G (p.Ile407Met)	FANCB, GLRA2 (I318M +1 more)	Single nucleotide variant (missense variant)	GLRA2-related disorder	GUncertain significance

ClinVar