ClinVar Miner

List of variants in gene NCAPH reported as uncertain significance for Microcephaly 23, primary, autosomal recessive

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_015341.5(NCAPH):c.1867G>A (p.Ala623Thr)	rs111936698	0.00096
NM_015341.5(NCAPH):c.1952T>C (p.Met651Thr)	rs2064714077	0.00001

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