List of variants in gene combination LOC132090059, PUS1 reported as likely benign for hematologic 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_025215.6(PUS1):c.397G>A (p.Asp133Asn)	rs76655496	0.00371
NM_025215.6(PUS1):c.364C>A (p.Arg122=)	rs142954643	0.00369

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