List of variants in gene combination LOC129935417, TMEM237 reported as likely pathogenic for cerebellar degeneration

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001044385.3(TMEM237):c.1A>G (p.Met1Val)	rs957203033	0.00003
NM_001044385.3(TMEM237):c.10_13dup (p.Ser5Ter)
NM_001044385.3(TMEM237):c.7_34del (p.Thr3fs)

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