ClinVar Miner

List of variants studied for hereditary spastic paraplegia 31 by Institute of Human Genetics, University of Leipzig Medical Center

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001371279.1(REEP1):c.329C>A (p.Ala110Glu) rs1182977563

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