Variant (rsID / SNP)

rs4046190

rs4046190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A15. Location: chromosome 1, position 116,534,852. The table records no clinical significance for this variant.

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Reference-table entries

SLC22A15Not classified

Variant type: synonymous_variant
Chromosome / position: 1:116534852
HGVS: NM_018420.3,c.288C>T,p.Ser96Ser
Allele change: Synonymous_S96S

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.