ClinVar Miner

List of variants in gene combination LOC111258526, NOS1 reported as uncertain significance for pyloric stenosis, infantile hypertrophic, 1

Included ClinVar conditions (1):

Pyloric stenosis, infantile hypertrophic, 1

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: 1

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HGVS	dbSNP	gnomAD frequency
NC_000012.12:g.117439680C>T	rs41279104	0.10627

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