List of variants in gene combination LOC130008755, TCTN1 reported as likely benign for Joubert syndrome; Meckel-Gruber syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001082538.3(TCTN1):c.220+12dup	rs1426313803	0.00001
NM_001082538.3(TCTN1):c.220+10A>C	rs1006963267
NM_001082538.3(TCTN1):c.220+11T>C	rs2548754700
NM_001082538.3(TCTN1):c.220+15C>A	rs773826085

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