List of variants in gene GRID2 reported as likely pathogenic for autosomal recessive spinocerebellar ataxia 18

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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_001510.4(GRID2):c.671G>A (p.Arg224Gln)	rs368143665	0.00001
NC_000004.11:g.(93511438_94006145)_(94006431_94031898)del
NM_001510.4(GRID2):c.910C>T (p.Arg304Ter)	rs1579319300

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