List of variants in gene SRP72 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006947.4(SRP72):c.1803G>A (p.Gly601=)	rs143643243	0.00131
NM_006947.4(SRP72):c.2004A>G (p.Lys668=)	rs148068843	0.00108
NM_006947.4(SRP72):c.1170T>C (p.Ser390=)	rs143262707	0.00085
NM_006947.4(SRP72):c.1704A>G (p.Pro568=)	rs41280351	0.00053
NM_006947.4(SRP72):c.1698T>C (p.Tyr566=)	rs145347209	0.00037
NM_006947.4(SRP72):c.406G>A (p.Val136Ile)	rs145817936	0.00028
NM_006947.4(SRP72):c.610+11T>C	rs558553825	0.00023
NM_006947.4(SRP72):c.1005C>T (p.Pro335=)	rs201570324	0.00019
NM_006947.4(SRP72):c.942T>A (p.Ala314=)	rs920124643	0.00001
NM_006947.4(SRP72):c.1119T>A (p.Ala373=)	rs2110124160
NM_006947.4(SRP72):c.1341G>A (p.Leu447=)
NM_006947.4(SRP72):c.1650T>C (p.Asp550=)	rs202073540
NM_006947.4(SRP72):c.1938C>T (p.His646=)	rs1721270142
NM_006947.4(SRP72):c.499-7_499-6del	rs2110113894

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