ClinVar Miner

List of variants reported as uncertain significance for MHC class II deficiency by New York Genome Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000246.4(CIITA):c.413T>C (p.Val138Ala)	rs142469968	0.00072
NM_003721.4(RFXANK):c.706C>T (p.Arg236Trp)	rs143964319	0.00053
NM_000246.4(CIITA):c.871G>A (p.Ala291Thr)	rs377598648	0.00002

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