List of variants in gene TMEM67 reported as benign for cerebellar ataxia

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_153704.6(TMEM67):c.1066-3C>T	rs3097427	0.65135
NM_153704.6(TMEM67):c.1810A>G (p.Ile604Val)	rs3134031	0.64845

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