ClinVar Miner

List of variants reported as benign for galactosemia by GeneReviews

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.652C>T (p.Leu218=)	rs2070075	0.02537
NM_000155.3(GALT):c.[652C>T;c.940A>G]
NM_000155.4(GALT):c.-119_-116delGTCA	rs111033640

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