ClinVar Miner

List of variants in gene combination LOC107648851, TAP2 reported as benign for MHC class I deficiency

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_000544.3(TAP2):c.658C>A (p.Arg220=) rs142794316

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