ClinVar Miner

List of variants in gene CNKSR2 reported as likely benign for Intellectual disability, X-linked, syndromic, Houge type

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_014927.5(CNKSR2):c.1497G>A (p.Lys499=)	rs144866575	0.00371
NM_014927.5(CNKSR2):c.2758A>C (p.Ser920Arg)	rs2147346551

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