List of variants in gene STIM1 reported as likely benign by GeneDx

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001382567.1(STIM1):c.969+167T>C	rs111991757	0.01235
NM_001382567.1(STIM1):c.792-59G>T	rs146231947	0.00902
NM_001382567.1(STIM1):c.139+246A>C	rs113897235	0.00833
NM_001382567.1(STIM1):c.*172A>G	rs3750996	0.00619
NM_001382567.1(STIM1):c.861C>T (p.Arg287=)	rs16929446	0.00556
NM_001382567.1(STIM1):c.1137+116T>C	rs16929441	0.00430
NM_003156.4(STIM1):c.1541+504T>C	rs79806392	0.00429
NM_001382567.1(STIM1):c.1239-13C>T	rs115353673	0.00426
NM_001382567.1(STIM1):c.1302G>A (p.Glu434=)	rs116837894	0.00426
NM_001382567.1(STIM1):c.1604C>T (p.Thr535Met)	rs146873551	0.00267
NM_001382567.1(STIM1):c.1634+269C>G	rs139558513	0.00229
NM_001382567.1(STIM1):c.1664C>T (p.Ser555Phe)	rs141215990	0.00163
NM_001382567.1(STIM1):c.386-11T>C	rs368922449	0.00028
NM_001382567.1(STIM1):c.597C>A (p.Leu199=)	rs189905382	0.00015
NM_001382567.1(STIM1):c.1634+11G>A	rs199732479	0.00011
NM_001382567.1(STIM1):c.1138-8C>T	rs750360122
NM_001382567.1(STIM1):c.1593G>A (p.Arg531=)	rs765806444
NM_001382567.1(STIM1):c.791+75C>G

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