List of variants in gene combination LOC130007233, SCNN1A, TNFRSF1A reported as likely benign for immune system disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
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_001065.4(TNFRSF1A):c.-96C>T	rs115164694	0.00312
NM_001065.4(TNFRSF1A):c.-74G>A	rs200084924	0.00003

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