List of variants in gene combination LCT, LOC126806353 reported as uncertain significance for nutritional disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002299.4(LCT):c.1461G>A (p.Ala487=)	rs146206234	0.00043
NM_002299.4(LCT):c.1396G>T (p.Gly466Trp)	rs377102890	0.00006
NM_002299.4(LCT):c.1045G>A (p.Glu349Lys)	rs886054868

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