ClinVar Miner

List of variants reported as pathogenic for MHC class II deficiency by Pathology and Clinical Laboratory Medicine, King Fahad Medical City

Included ClinVar conditions (2):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003721.4(RFXANK):c.362A>T (p.Asp121Val)	rs104894709
NM_003721.4(RFXANK):c.558T>A (p.Tyr186Ter)	rs1599784374

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