ClinVar Miner

List of variants in gene SLC38A8 reported by Fulgent Genetics, Fulgent Genetics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001080442.3(SLC38A8):c.190-8C>T	rs1876961	0.00719
NM_001080442.3(SLC38A8):c.598C>T (p.Gln200Ter)	rs149592537	0.00001

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