List of variants in gene SP7 reported as uncertain significance by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001173467.3(SP7):c.839G>T (p.Arg280Leu)	rs200582631	0.00026
NM_001173467.3(SP7):c.799C>T (p.Arg267Cys)	rs201666834	0.00019
NM_001173467.3(SP7):c.855G>A (p.Ala285=)	rs561083858	0.00007
NM_001173467.3(SP7):c.1184G>A (p.Arg395His)	rs369792296	0.00004
NM_001173467.3(SP7):c.184G>T (p.Asp62Tyr)	rs2136836404
NM_001173467.3(SP7):c.500G>A (p.Trp167Ter)	rs1294471020
NM_001173467.3(SP7):c.675C>T (p.Pro225=)	rs1250981237

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