List of variants in gene combination LOC130009809, RNASEH2B reported as likely benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024570.4(RNASEH2B):c.-112C>T	rs184573722	0.00678
NM_024570.4(RNASEH2B):c.-117C>G	rs553446261	0.00094

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