Variant (rsID / SNP)

rs201443231

rs201443231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC13A3. Location: chromosome 20, position 45,242,184. Clinical significance in the table: Benign.

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Reference-table entries

SLC13A3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:45242184
Cytoband: 20q13.12
HGVS: NM_022829.6(SLC13A3):c.292A>T (p.Ile98Phe)
Allele change: Missense_I98F

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.