C1858266[trait identifier] AND "Women's Health and Genetics/Laboratory - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2501118	NM_001290043.2(TAP2):c.814_815delinsC (p.Leu272fs)	TAP2 (L272fs)	Indel (frameshift variant)	MHC class I deficiency	GLikely pathogenic
Select item 937287	NM_000593.6(TAP1):c.-46_-45delinsAT	TAP1	Indel (5 prime UTR variant)	MHC class I deficiency	GPathogenic/Likely pathogenic