Variant (rsID / SNP)

rs2140516

rs2140516 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC13A1. Location: chromosome 7, position 122,809,234. The table records no clinical significance for this variant.

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Reference-table entries

SLC13A1Not classified

Variant type: missense_variant
Chromosome / position: 7:122809234
HGVS: NM_022444.4,c.521A>G,p.Asn174Ser
Allele change: Missense_N174S

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.