List of variants in gene CTRC reported as benign by Ambry Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_007272.3(CTRC):c.514A>G (p.Lys172Glu)	rs34949635	0.02786
NM_007272.3(CTRC):c.285C>T (p.Asp95=)	rs41307798	0.02352
NM_007272.3(CTRC):c.156C>T (p.Asn52=)	rs77373944	0.00830
NM_007272.3(CTRC):c.690G>A (p.Glu230=)	rs75971387	0.00820
NM_007272.3(CTRC):c.110G>A (p.Arg37Gln)	rs145868278	0.00032
NM_007272.3(CTRC):c.180C>T (p.Gly60=)	rs497078

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