Variant (rsID / SNP)

rs4833095

rs4833095 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR1. Location: chromosome 4, position 38,799,710. Clinical significance in the table: risk factor.

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Reference-table entries

TLR1Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 4:38799710
Cytoband: 4p14
HGVS: NM_003263.4(TLR1):c.743A>G (p.Asn248Ser)
Allele change: Missense_N248S

Associated conditions / phenotypes

Leprosy, susceptibility to, 5

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.