List of variants in gene SLC25A19 reported as benign for thiamine-responsive dysfunction syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001126121.2(SLC25A19):c.289-26G>A	rs4788882	0.99234
NM_001126121.2(SLC25A19):c.339T>C (p.Tyr113=)	rs7213318	0.93459
NM_001126121.2(SLC25A19):c.-155T>G	rs2291033	0.90349

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