List of variants in gene SEC24D reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_014822.4(SEC24D):c.248+7T>C	rs139956480	0.00513
NM_014822.4(SEC24D):c.599C>T (p.Pro200Leu)	rs114096530	0.00287
NM_014822.4(SEC24D):c.181C>A (p.Pro61Thr)	rs143180885	0.00162
NM_014822.4(SEC24D):c.755C>T (p.Pro252Leu)	rs372402939	0.00006
NM_014822.4(SEC24D):c.153C>T (p.Thr51=)

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