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Variant (rsID / SNP)

rs4073918

SLC6A18

rs4073918 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC6A18. Location: chromosome 5, position 1,244,425. The table records no clinical significance for this variant.

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Reference-table entries

SLC6A18Not classified
Variant type
missense_variant
Chromosome / position
5:1244425
HGVS
NM_182632.3,c.1433C>T,p.Pro478Leu
Allele change
Missense_P478L

Public references

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