Variant (rsID / SNP)

rs17248

rs17248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRBV10-1. Location: chromosome 7, position 142,231,701. The table records no clinical significance for this variant.

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Reference-table entries

TRBV10-1Not classified

Variant type: missense_variant
Chromosome / position: 7:142231701
HGVS: unassigned_transcript_1330,c.216C>A,p.His72Gln

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.