ClinVar Miner

List of variants in gene STAG2 reported as uncertain significance for not specified

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_001042750.2(STAG2):c.2924+5T>A	rs1230977778	0.00003
NM_001042750.2(STAG2):c.3052G>A (p.Val1018Met)	rs2059016659

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