ClinVar Miner

List of variants in gene combination LOC130067862, SCO2, TYMP reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001953.5(TYMP):c.1127G>A (p.Arg376Gln)	rs765007158	0.00024
NM_001953.4(TYMP):c.929-6_929-3del	rs201685922

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