Variant (rsID / SNP)

rs117660448

rs117660448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TENT5A. Location: chromosome 6, position 82,461,874. The table records no clinical significance for this variant.

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Reference-table entries

TENT5ANot classified

Variant type: 5_prime_UTR_variant
Chromosome / position: 6:82461874
HGVS: NM_017633.3,c.-16G>T
Allele change: Silent

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.