ClinVar Miner

List of variants in gene combination LOC129933675, MCFD2 reported as uncertain significance for Factor 5 and Factor VIII, combined deficiency of, 2

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001171506.2(MCFD2):c.-189C>G	rs886056125	0.02167
NM_001171506.2(MCFD2):c.-205G>C	rs1382510299	0.00054

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