Variant (rsID / SNP)

rs143813189

rs143813189 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAF3. Location: chromosome 14, position 103,342,015. Clinical significance in the table: Likely benign.

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Reference-table entries

TRAF3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:103342015
Cytoband: 14q32.32
HGVS: NM_145725.3(TRAF3):c.352C>T (p.Arg118Trp)
Allele change: Missense_R118W

Associated conditions / phenotypes

Herpes simplex encephalitis, susceptibility to, 3

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.