ClinVar Miner

List of variants in gene combination LOC129937857, PDCD10 reported as uncertain significance for cerebral cavernous malformation

Included ClinVar conditions (8):

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_007217.4(PDCD10):c.-393G>A	rs779552942	0.00012
NM_007217.4(PDCD10):c.-432C>T	rs886058164	0.00007

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