ClinVar Miner

List of variants reported as pathogenic for autosomal recessive spinocerebellar ataxia 18 by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
GRCh38/hg38 4q22.1(chr4:92303869-92304842)x0

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