List of variants in gene SLC16A1 reported as likely pathogenic for not provided

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003051.4(SLC16A1):c.490dup (p.Leu164fs)	rs606231312
NM_003051.4(SLC16A1):c.499del (p.Val167fs)	rs606231301
NM_003051.4(SLC16A1):c.727C>T (p.Arg243Ter)	rs2101621602
NM_003051.4(SLC16A1):c.764T>G (p.Leu255Ter)

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