List of variants in gene combination NANS, TRIM14 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_018946.4(NANS):c.870+53A>G	rs4237190	0.60836
NM_018946.4(NANS):c.153T>C (p.Ala51=)	rs13049	0.60644
NM_018946.4(NANS):c.102C>T (p.Asp34=)	rs3739670	0.32810
NM_018946.4(NANS):c.133-124G>A	rs7846880	0.32510
NM_018946.4(NANS):c.348+81C>A	rs7020081	0.29875
NM_018946.4(NANS):c.870+296C>A	rs16912622	0.29514
NM_018946.4(NANS):c.204G>C (p.Glu68Asp)	rs1058446	0.22045
NM_018946.4(NANS):c.870+4T>C	rs41424445	0.00613
NM_018946.4(NANS):c.520C>T (p.Pro174Ser)	rs115305859	0.00475

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