ClinVar Miner

List of variants in gene SLC33A1 studied for Spastic paraplegia, autosomal dominant

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004733.4(SLC33A1):c.1673_1676del	rs143606890
NM_004733.4(SLC33A1):c.582_583del	rs762573505
NM_004733.4(SLC33A1):c.*893del	rs886058103

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