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Variant (rsID / SNP)

rs8135665

SLC16A8

rs8135665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A8. Location: chromosome 22, position 38,476,276. The table records no clinical significance for this variant.

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Reference-table entries

SLC16A8Not classified
Variant type
single nucleotide variant
Chromosome / position
22:38476276
Cytoband
22q13.1
HGVS
NM_013356.3(SLC16A8):c.1198+571G>A
Allele change
Silent

Public references

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