List of variants in gene SLC16A1 reported as likely benign for carbohydrate metabolism disease

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_003051.4(SLC16A1):c.*145T>G	rs11585690	0.01723
NM_003051.4(SLC16A1):c.*1876G>C	rs11811205	0.01235
NM_003051.4(SLC16A1):c.*332T>C	rs41306207	0.01211
NM_003051.4(SLC16A1):c.1002G>A (p.Ala334=)	rs114731222	0.00609
NM_003051.4(SLC16A1):c.973A>G (p.Ile325Val)	rs116216229	0.00409
NM_003051.4(SLC16A1):c.*1281T>G	rs184445532	0.00263
NM_003051.4(SLC16A1):c.1282G>A (p.Val428Ile)	rs536012651	0.00048
NM_003051.4(SLC16A1):c.*1624A>G	rs140456426	0.00027
NM_003051.4(SLC16A1):c.404T>C (p.Ile135Thr)	rs1570620206	0.00001
NM_003051.4(SLC16A1):c.362-58TATT[8]	rs149491709

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