List of variants in gene combination HPS5, LOC126861152 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_181507.1(HPS5):c.-251C>A	rs4150530	0.13814
NM_181507.2(HPS5):c.-142C>T	rs4150528	0.00903
NM_181507.1(HPS5):c.-250G>T	rs4150529	0.00728
NM_181507.2(HPS5):c.-91C>G	rs4150527	0.00513

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