ClinVar Miner

List of variants in gene combination ANO10, LOC129936579 reported as uncertain significance for Autosomal recessive cerebellar ataxia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_018075.4(ANO10):c.-140G>A	rs886058485	0.00002
NM_018075.5(ANO10):c.-95del	rs886058483

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