List of variants in gene SEPSECS reported as 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_016955.4(SEPSECS):c.1356G>C (p.Lys452Asn)	rs2302566	0.07763
NM_016955.4(SEPSECS):c.1211+7A>G	rs17408685	0.04557
NM_016955.4(SEPSECS):c.1394G>A (p.Arg465Gln)	rs115959591	0.00697
NM_016955.4(SEPSECS):c.780A>G (p.Ser260=)	rs61747281	0.00120
NM_016955.4(SEPSECS):c.115-18dup	rs34423002

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