Variant (rsID / SNP)

rs13278062

rs13278062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC111255645, TNFRSF10A, TNFRSF10A-DT. Location: chromosome 8, position 23,082,971. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LOC111255645Not classified

Variant type: single nucleotide variant
Chromosome / position: 8:23082971
Cytoband: 8p21.3
HGVS: NR_033928.1(TNFRSF10A-DT):n.238G>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.