Variant (rsID / SNP)

rs141240817

rs141240817 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFITM5. Location: chromosome 11, position 298,622. Clinical significance in the table: Benign.

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Reference-table entries

IFITM5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:298622
Cytoband: 11p15.5
HGVS: NM_001025295.3(IFITM5):c.278C>T (p.Thr93Met)
Allele change: Missense_T93M

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.