ClinVar Miner

List of variants in gene GRID2 reported as uncertain significance for autosomal recessive spinocerebellar ataxia 18

Included ClinVar conditions (1):
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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_001510.4(GRID2):c.899G>A (p.Arg300His) rs201635818 0.00003
NM_001510.4(GRID2):c.-62C>T
NM_001510.4(GRID2):c.101A>G (p.Asp34Gly)
NM_001510.4(GRID2):c.1100G>A (p.Arg367His)
NM_001510.4(GRID2):c.121G>T (p.Asp41Tyr) rs1728640535
NM_001510.4(GRID2):c.1658A>G (p.Glu553Gly) rs752073311
NM_001510.4(GRID2):c.2921T>A (p.Phe974Tyr)
NM_001510.4:c.1246-278_2193+35240del
NM_001510.4:c.790-271_1245+268del

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