List of variants in gene CNKSR2 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_014927.5(CNKSR2):c.651A>G (p.Gln217=)	rs77732468	0.01503
NM_014927.5(CNKSR2):c.2983G>A (p.Asp995Asn)	rs138982878	0.01442
NM_014927.5(CNKSR2):c.525T>C (p.Cys175=)	rs34161348	0.01010
NM_014927.5(CNKSR2):c.2926C>T (p.Leu976=)	rs145113843	0.00209

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