ClinVar Miner

List of variants in gene NCAPH2 reported as not provided by GenomeConnect - Brain Gene Registry

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_152299.4(NCAPH2):c.964C>T (p.Pro322Ser)	rs138253876	0.00052
NM_152299.4(NCAPH2):c.325G>A (p.Gly109Arg)	rs372044931	0.00006

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