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Variant (rsID / SNP)

rs62636569

SLC6A17

rs62636569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC6A17. Location: chromosome 1, position 110,735,290. The table records no clinical significance for this variant.

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Reference-table entries

SLC6A17Not classified
Variant type
synonymous_variant
Chromosome / position
1:110735290
HGVS
NM_001010898.4,c.1269C>T,p.Asp423Asp
Allele change
Synonymous_D423D

Public references

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