List of variants in gene SNCAIP reported as likely benign by Labcorp Genetics (formerly Invitae), Labcorp

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_005460.4(SNCAIP):c.217T>C (p.Phe73Leu)	rs142172029	0.00136
NM_005460.4(SNCAIP):c.111G>A (p.Thr37=)	rs10070158	0.00098
NM_005460.4(SNCAIP):c.240G>A (p.Ser80=)	rs147854746	0.00021
NM_005460.4(SNCAIP):c.951A>G (p.Lys317=)	rs372022750	0.00005
NM_005460.4(SNCAIP):c.438C>T (p.Tyr146=)	rs150946460	0.00002

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