List of variants in gene STIM1 reported as not provided

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001382567.1(STIM1):c.1080A>G (p.Gln360=)	rs2304891	0.43325
NM_001382567.1(STIM1):c.1382T>C (p.Met461Thr)	rs1444907403	0.00003
NM_001382567.1(STIM1):c.216C>G (p.His72Gln)	rs397515436
NM_001382567.1(STIM1):c.700_707del (p.Asn234fs)	rs1590688717
NM_001382567.1(STIM1):c.910C>T (p.Arg304Trp)	rs483352867

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