ClinVar Miner

List of variants reported as likely pathogenic for Global developmental delay; Seizures; Intellectual disability; CNS hypomyelination; Brain atrophy; Muscular hypotonia

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Total variants: 2
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HGVS dbSNP
NM_000844.3(GRM7):c.1972C>T (p.Arg658Trp) rs1114167300
NM_000844.3(GRM7):c.2024C>A (p.Thr675Lys) rs1114167301

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