List of variants in gene CNKSR2 reported as uncertain significance by Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014927.5(CNKSR2):c.2666C>A (p.Ala889Glu)	rs893893504	0.00001
NM_014927.5(CNKSR2):c.1030G>A (p.Asp344Asn)
NM_014927.5(CNKSR2):c.2680A>G (p.Ile894Val)	rs930186060

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