ClinVar Miner

List of variants in gene SAR1B reported as not provided for chylomicron retention disease

Included ClinVar conditions (1):

Chylomicron retention disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_016103.4(SAR1B):c.409G>A (p.Asp137Asn)	rs28942109	0.00004
NM_016103.4(SAR1B):c.537T>A (p.Ser179Arg)	rs28942110	0.00001

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