List of variants in gene combination LOC129935417, TMEM237 reported as likely benign 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.15G>C (p.Ser5=)	rs879874108	0.00003
NM_001044385.3(TMEM237):c.-25G>A	rs568671275
NM_001044385.3(TMEM237):c.24G>A (p.Arg8=)	rs377090903

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