Variant (rsID / SNP)

rs2292151

rs2292151 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TICAM1. Location: chromosome 19, position 4,816,719. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TICAM1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:4816719
Cytoband: 19p13.3
HGVS: NM_182919.4(TICAM1):c.1671C>T (p.Asp557=)
Allele change: Synonymous_D557D

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.