"Illumina Laboratory Services, Illumina"[submitter] AND "TTC21B-AS1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 198257	NM_024753.5(TTC21B):c.691A>T (p.Thr231Ser)	TTC21B, TTC21B-AS1 (T231S)	Single nucleotide variant (missense variant)	TTC21B-related condition +7 more	GConflicting classifications of pathogenicity
Select item 893757	NM_024753.5(TTC21B):c.685G>A (p.Asp229Asn)	TTC21B, TTC21B-AS1 (D229N)	Single nucleotide variant (missense variant)	Nephronophthisis 12 +1 more	GUncertain significance
Select item 130658	NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu)	TTC21B-AS1, TTC21B (Q222L)	Single nucleotide variant (missense variant)	not specified +6 more	GBenign/Likely benign
Select item 130657	NM_024753.5(TTC21B):c.601G>A (p.Val201Met)	TTC21B, TTC21B-AS1 (V201M)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign
Select item 331839	NM_024753.5(TTC21B):c.481A>G (p.Thr161Ala)	TTC21B-AS1, TTC21B (T161A)	Single nucleotide variant (missense variant)	Nephronophthisis 12 +4 more	GConflicting classifications of pathogenicity
Select item 894674	NM_024753.5(TTC21B):c.338A>G (p.His113Arg)	TTC21B, TTC21B-AS1 (H113R)	Single nucleotide variant (missense variant)	TTC21B-related condition +4 more	GConflicting classifications of pathogenicity

ClinVar