Variant (rsID / SNP)

rs7255265

rs7255265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TICAM1. Location: chromosome 19, position 4,818,378. Clinical significance in the table: Benign.

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Reference-table entries

TICAM1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:4818378
Cytoband: 19p13.3
HGVS: NM_182919.4(TICAM1):c.12A>G (p.Thr4=)
Allele change: Synonymous_T4T

Associated conditions / phenotypes

Herpes simplex encephalitis, susceptibility to, 4

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.