Variant (rsID / SNP)

rs137853178

rs137853178 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR6. Location: chromosome 4, position 38,830,713. The table records no clinical significance for this variant.

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Reference-table entries

TLR6Not classified

Variant type: single nucleotide variant
Chromosome / position: 4:38830713
Cytoband: 4p14
HGVS: NM_006068.5(TLR6):c.382C>G (p.Leu128Val)
Allele change: Missense_L128V

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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