List of variants in gene SLC33A1 reported as likely benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004733.4(SLC33A1):c.1482+7A>G	rs149522913	0.00458
NM_004733.4(SLC33A1):c.1525G>A (p.Gly509Ser)	rs76440173	0.00267
NM_004733.4(SLC33A1):c.136G>A (p.Glu46Lys)	rs149571533	0.00190
NM_004733.4(SLC33A1):c.1451A>C (p.Asn484Thr)	rs144015992	0.00190
NM_004733.4(SLC33A1):c.1569T>C (p.Gly523=)	rs150442784

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