ClinVar Miner

List of variants in gene DDHD1 reported as uncertain significance by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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_001160148.2(DDHD1):c.340T>C (p.Ser114Pro)	rs756788863	0.00011
NM_001160148.2(DDHD1):c.53GCG[6] (p.Gly22dup)	rs752119831

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