Variant (rsID / SNP)

rs2075496

rs2075496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAV36DV7. Location: chromosome 14, position 22,694,926. The table records no clinical significance for this variant.

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Reference-table entries

TRAV36DV7Not classified

Variant type: synonymous_variant
Chromosome / position: 14:22694926
HGVS: unassigned_transcript_2184,c.117C>T,p.Thr39Thr

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.