ClinVar Miner

List of variants in gene ABCC6 reported as pathogenic for See cases

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_001171.6(ABCC6):c.3421C>T (p.Arg1141Ter)	rs72653706	0.00122
NM_001171.6(ABCC6):c.3490C>T (p.Arg1164Ter)	rs72653744	0.00012

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