ClinVar Miner

List of variants in gene combination DEAF1, LOC126861109 reported as uncertain significance by Revvity Omics, Revvity

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_021008.4(DEAF1):c.1318G>A (p.Ala440Thr)	rs149746031	0.00006
NM_021008.4(DEAF1):c.1489G>C (p.Ala497Pro)	rs762338624

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