ClinVar Miner

List of variants in gene UNG 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_080911.3(UNG):c.*500C>G	rs780337127
NM_080911.3(UNG):c.*866AT[5]	rs56185014

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