ClinVar Miner

List of variants reported as likely benign for A20 haploinsufficiency by Genetics and Molecular Pathology, SA Pathology

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001270508.2(TNFAIP3):c.322A>G (p.Thr108Ala)	rs376205580	0.00033
NM_001270508.2(TNFAIP3):c.619A>C (p.Ile207Leu)	rs141807543	0.00013

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