ClinVar Miner

List of variants in gene SLC38A8 reported by Undiagnosed Diseases Network, NIH

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.848A>C (p.Asp283Ala)	rs139373929	0.00024
NM_001080442.3(SLC38A8):c.913T>C (p.Ser305Pro)	rs1057521634

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