ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001510.4(GRID2):c.1251T>G (p.Gly417=) rs1385405 0.72183
NM_001510.4(GRID2):c.735+21G>C rs2271385

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