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Variant (rsID / SNP)

rs11466649

TLR10

rs11466649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR10. Location: chromosome 4, position 38,776,725. The table records no clinical significance for this variant.

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Reference-table entries

TLR10Not classified
Variant type
missense_variant
Chromosome / position
4:38776725
HGVS
NM_001017388.3,c.487G>T,p.Ala163Ser
Allele change
Missense_A163S

Associated conditions / phenotypes

Bone Inflammation Disease

Public references

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