Variant (rsID / SNP)

rs9842091

rs9842091 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A13. Location: chromosome 3, position 38,307,510. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A13Not classified

Variant type: synonymous_variant
Chromosome / position: 3:38307510
HGVS: NM_004256.4,c.159T>C,p.Ala53Ala
Allele change: Synonymous_A53A

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.