List of variants in gene STIM1 reported as pathogenic by Invitae

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: 13

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.(?_4059271)_(4059406_?)del
NC_000011.9:g.(?_3988762)_(4113028_?)del
NC_000011.9:g.(?_4076736)_(4076887_?)del
NM_001382567.1(STIM1):c.1189del (p.Ala397fs)	rs2133224258
NM_001382567.1(STIM1):c.1285C>T (p.Arg429Cys)	rs397514671
NM_001382567.1(STIM1):c.1452del (p.Ile484fs)	rs1565171115
NM_001382567.1(STIM1):c.1463T>A (p.Leu488Ter)
NM_001382567.1(STIM1):c.163_164del (p.Leu55fs)	rs2135736277
NM_001382567.1(STIM1):c.326A>G (p.His109Arg)	rs397514677
NM_001382567.1(STIM1):c.343A>T (p.Ile115Phe)	rs527236030
NM_001382567.1(STIM1):c.700_707del (p.Asn234fs)	rs1590688717
NM_001382567.1(STIM1):c.869_887del (p.Ile290fs)	rs751733169
NM_001382567.1(STIM1):c.910C>T (p.Arg304Trp)	rs483352867

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