List of variants in gene combination POMGNT1, TSPAN1 reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_017739.4(POMGNT1):c.1284+9G>C	rs565797493	0.00026
NM_017739.4(POMGNT1):c.1285-6C>T	rs377292905	0.00009
NM_017739.4(POMGNT1):c.550C>T (p.His184Tyr)	rs746638187	0.00005
NM_017739.4(POMGNT1):c.1783A>G (p.Lys595Glu)	rs797045896	0.00003
NM_017739.4(POMGNT1):c.440G>A (p.Arg147His)	rs776165339	0.00003
NM_017739.4(POMGNT1):c.1142A>G (p.Asn381Ser)	rs140846775	0.00002
NM_017739.4(POMGNT1):c.1456C>G (p.Arg486Gly)	rs534543454
NM_017739.4(POMGNT1):c.461C>A (p.Pro154His)	rs886043030

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