ClinVar Miner

List of variants in gene combination CDC42, LOC122056785 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001791.4(CDC42):c.487-1465T>A	rs2522245188

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