List of variants in gene SIGLEC11 reported as likely benign by Ambry Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_052884.3(SIGLEC11):c.64G>A (p.Val22Met)	rs562231084	0.00049
NM_052884.3(SIGLEC11):c.1214G>A (p.Arg405Gln)	rs772490728	0.00018
NM_052884.3(SIGLEC11):c.1120G>A (p.Gly374Arg)	rs577987618	0.00013
NM_052884.3(SIGLEC11):c.9G>A (p.Pro3=)	rs371271734	0.00006
NM_052884.3(SIGLEC11):c.1708G>A (p.Ala570Thr)	rs767835963	0.00003
NM_052884.3(SIGLEC11):c.1664A>G (p.His555Arg)	rs1038111334
NM_052884.3(SIGLEC11):c.1741G>A (p.Val581Ile)	rs140702198
NM_052884.3(SIGLEC11):c.673G>A (p.Asp225Asn)
NM_052884.3(SIGLEC11):c.965G>C (p.Arg322Pro)	rs201747553
NM_052884.3(SIGLEC11):c.974G>A (p.Arg325Lys)	rs1245376830

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