List of variants in gene combination LOC130067862, SCO2, TYMP reported as benign for spinal muscular atrophy

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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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.972C>T (p.Ala324=)	rs131804	0.51130
NM_001953.5(TYMP):c.1412C>T (p.Ser471Leu)	rs11479	0.09354

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