List of variants in gene combination LOC130005165, STIM1 reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001382567.1(STIM1):c.13G>A (p.Val5Ile)	rs150529970
NM_001382567.1(STIM1):c.4G>A (p.Asp2Asn)	rs2090364498
NM_001382567.1(STIM1):c.7G>A (p.Val3Ile)	rs1060499904

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