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Variant (rsID / SNP)

rs11466653

TLR10

rs11466653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR10. Location: chromosome 4, position 38,776,235. The table records no clinical significance for this variant.

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Reference-table entries

TLR10Not classified
Variant type
missense_variant
Chromosome / position
4:38776235
HGVS
NM_001017388.3,c.977T>C,p.Met326Thr
Allele change
Missense_M326T

Associated conditions / phenotypes

Thyroid Cancer, Nonmedullary, 1|Thyroid Carcinoma|Bone Inflammation Disease

Public references

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