List of variants in gene SNAP29 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004782.4(SNAP29):c.629C>T (p.Ser210Phe)	rs141934766	0.00076
NM_004782.4(SNAP29):c.51C>G (p.Asp17Glu)	rs375076880	0.00029
NM_004782.4(SNAP29):c.318G>C (p.Gln106His)	rs201300635	0.00002
NM_004782.4(SNAP29):c.58G>C (p.Ala20Pro)	rs765170256	0.00001
NM_004782.4(SNAP29):c.145G>A (p.Val49Ile)	rs2147855039
NM_004782.4(SNAP29):c.16A>G (p.Lys6Glu)	rs1046897856
NM_004782.4(SNAP29):c.22T>C (p.Tyr8His)	rs2147854587

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