List of variants in gene CREB3L1 reported as uncertain significance by GeneDx

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_052854.4(CREB3L1):c.284C>T (p.Ala95Val)	rs190038304	0.00110
NM_052854.4(CREB3L1):c.274G>A (p.Gly92Ser)	rs200839792	0.00073
NM_052854.4(CREB3L1):c.1105G>A (p.Ala369Thr)	rs201046043	0.00025
NM_052854.4(CREB3L1):c.1109C>T (p.Thr370Ile)	rs776460030	0.00003
NM_052854.4(CREB3L1):c.667C>T (p.Arg223Cys)	rs745567388	0.00003
NM_052854.4(CREB3L1):c.46G>T (p.Gly16Ter)	rs1555221055	0.00001
NM_052854.4(CREB3L1):c.488C>G (p.Pro163Arg)	rs747612049
NM_052854.4(CREB3L1):c.922C>T (p.Arg308Cys)	rs768811137

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