List of variants in gene LCT reported as benign for digestive system disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002299.4(LCT):c.*50G>C	rs1042712	0.78588
NM_002299.4(LCT):c.4606C>T (p.Leu1536=)	rs2304371	0.69539
NM_002299.4(LCT):c.5568T>C (p.Ala1856=)	rs2278544	0.60314
NM_002299.4(LCT):c.4916A>G (p.Asn1639Ser)	rs2322659	0.59219
NM_002299.4(LCT):c.582C>T (p.Thr194=)	rs2236783	0.51423
NM_002299.4(LCT):c.4329C>T (p.Gly1443=)	rs3739022	0.15421
NM_002299.4(LCT):c.655G>A (p.Val219Ile)	rs3754689

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