List of variants in gene LCT reported as benign for Congenital lactase deficiency

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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: 17

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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.4465-37C>T	rs2304370	0.23782
NM_002299.4(LCT):c.5111+23C>T	rs3213890	0.18490
NM_002299.4(LCT):c.4329C>T (p.Gly1443=)	rs3739022	0.15421
NM_002299.4(LCT):c.4977-26T>C	rs3213891	0.03191
NM_002299.4(LCT):c.454G>A (p.Ala152Thr)	rs114525655	0.01314
NM_002299.4(LCT):c.*325G>C	rs62170085	0.01267
NM_002299.4(LCT):c.301A>G (p.Ser101Gly)	rs35837297	0.00812
NM_002299.4(LCT):c.4347T>C (p.Phe1449=)	rs17699796	0.00774
NM_002299.4(LCT):c.4777G>A (p.Val1593Met)	rs35891837	0.00726
NM_002299.4(LCT):c.2763G>A (p.Ala921=)	rs116951780	0.00313
NM_002299.4(LCT):c.318C>T (p.Asp106=)	rs34307240
NM_002299.4(LCT):c.655G>A (p.Val219Ile)	rs3754689

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