List of variants in gene SLC13A3 reported as uncertain significance for acute 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022829.6(SLC13A3):c.1637G>A (p.Arg546Gln)	rs188700676	0.00011
NM_022829.6(SLC13A3):c.1106G>A (p.Ser369Asn)	rs758830291	0.00003
NM_022829.6(SLC13A3):c.86C>T (p.Pro29Leu)	rs1381905345	0.00002
NM_022829.6(SLC13A3):c.1757A>G (p.Asn586Ser)	rs201877988	0.00001

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