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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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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
NC_000009.12:g.98056438C>T	rs6478539	0.31469
NM_018946.4(NANS):c.871-121A>G	rs2281732	0.30718
NM_018946.4(NANS):c.348+81C>A	rs7020081	0.29875
NM_018946.4(NANS):c.133-224T>A	rs7038592	0.29828
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+7C>G	rs7030291	0.01483
NM_018946.4(NANS):c.870+4T>C	rs41424445	0.00613
NM_018946.4(NANS):c.520C>T (p.Pro174Ser)	rs115305859	0.00475
NM_018946.4(NANS):c.744T>C (p.Ser248=)	rs148983734	0.00182
NM_018946.4(NANS):c.351G>A (p.Met117Ile)	rs143387431	0.00131
NM_018946.4(NANS):c.684G>A (p.Val228=)	rs374656906	0.00048
NM_018946.4(NANS):c.1045T>C (p.Leu349=)	rs34342219
NM_018946.4(NANS):c.603+19dup	rs2490397878

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