List of variants in gene CORO1A reported as likely pathogenic for T-B+ severe combined immunodeficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_007074.4(CORO1A):c.1007+1G>A	rs2151063274
NM_007074.4(CORO1A):c.1065+2T>C	rs112728974
NM_007074.4(CORO1A):c.35G>T (p.Arg12Leu)	rs2543751507

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