List of variants in gene combination FAM219B, MPI reported as uncertain significance for immune system disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002435.3(MPI):c.*312T>A	rs545401402	0.00086
NM_002435.3(MPI):c.*289A>G	rs1405523963	0.00006
NM_002435.3(MPI):c.*441G>C	rs1042476793	0.00001
NM_002435.3(MPI):c.*483G>C	rs886051486	0.00001
NM_002435.3(MPI):c.*393G>A	rs886051485

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