Variant (rsID / SNP)

rs2272550

rs2272550 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAV26-1. Location: chromosome 14, position 22,591,988. The table records no clinical significance for this variant.

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Reference-table entries

TRAV26-1Not classified

Variant type: missense_variant
Chromosome / position: 14:22591988
HGVS: unassigned_transcript_2172,c.73C>A,p.Pro25Thr

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.