List of variants in gene JCAD reported as 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_020848.4(JCAD):c.78C>G (p.Asn26Lys)	rs76425998	0.01754
NM_020848.4(JCAD):c.3896C>T (p.Pro1299Leu)	rs76622613	0.00606
NM_020848.4(JCAD):c.372G>A (p.Arg124=)	rs41284752	0.00500
NM_020848.4(JCAD):c.3855C>T (p.Ala1285=)	rs117029734	0.00449
NM_020848.4(JCAD):c.3838G>A (p.Asp1280Asn)	rs61741026

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