"Invitae"[submitter] AND "RORB-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2770599	NM_006914.4(RORB):c.2T>G (p.Met1Arg)	RORB, RORB-AS1 (M1R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2825215	NM_006914.4(RORB):c.3G>C (p.Met1Ile)	RORB, RORB-AS1 (M1I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1483936	NM_006914.4(RORB):c.5G>C (p.Arg2Pro)	RORB, RORB-AS1 (R2P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1695250	NM_006914.4(RORB):c.7+6C>T	RORB, RORB-AS1	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 2831046	NM_006914.4(RORB):c.7+15G>C	RORB, RORB-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1610805	NM_006914.4(RORB):c.7+20C>T	RORB, RORB-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1528222	NM_006914.4(RORB):c.7+20C>A	RORB, RORB-AS1	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar