Variant (rsID / SNP)

rs8177374

rs8177374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TIRAP. Location: chromosome 11, position 126,162,843. Clinical significance in the table: Benign.

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Reference-table entries

TIRAPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:126162843
Cytoband: 11q24.2
HGVS: NM_001318777.2(TIRAP):c.539C>T (p.Ser180Leu)
Allele change: Missense_S180L

Associated conditions / phenotypes

Invasive pneumococcal disease, protection against|Malaria, resistance to|Mycobacterium tuberculosis, protection against|Bacteremia, susceptibility

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.