ClinVar Miner

List of variants reported as likely pathogenic for VEXAS syndrome by MGZ Medical Genetics Center

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_003334.4(UBA1):c.121A>C (p.Met41Leu)	rs1936307795
NM_003334.4(UBA1):c.121A>G (p.Met41Val)	rs1936307795
NM_003334.4(UBA1):c.122T>C (p.Met41Thr)	rs782416867

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