List of variants in gene AICDA reported as uncertain significance for Hyperimmunoglobulin M syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020661.4(AICDA):c.1453_1454insG	rs201738977	0.01403
NM_020661.4(AICDA):c.428-4_428-3insT	rs755095913	0.00272
NM_020661.4(AICDA):c.428-17_428-16dup	rs5796316

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