List of variants in gene TMEM237 reported as likely pathogenic for Joubert syndrome and related disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001044385.3(TMEM237):c.553+1G>A	rs80034299	0.00002
NM_001044385.3(TMEM237):c.636G>A (p.Trp212Ter)	rs2105899200
NM_001044385.3(TMEM237):c.725G>A (p.Trp242Ter)

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