List of variants in gene combination LOC124418421, STIM1 reported as benign for hematologic disorder

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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_001382567.1(STIM1):c.1931C>A (p.Ser644Tyr)	rs35637264	0.00323
NM_001382567.1(STIM1):c.1896C>G (p.Pro632=)	rs61743670	0.00212

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