ClinVar Miner

List of variants in gene ATP11C reported as pathogenic for X-linked congenital hemolytic anemia

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_001353812.2(ATP11C):c.1244C>A (p.Thr415Asn)	rs1556323334
NM_001353812.2(ATP11C):c.1666+2T>C	rs2148723294

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