Variant (rsID / SNP)

rs2230229

rs2230229 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF10A. Location: chromosome 8, position 23,049,292. The table records no clinical significance for this variant.

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Reference-table entries

TNFRSF10ANot classified

Variant type: missense_variant
Chromosome / position: 8:23049292
HGVS: NM_003844.4,c.1322G>A,p.Arg441Lys
Allele change: Missense_R441K

Associated conditions / phenotypes

Lymphoma|Follicular Lymphoma

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.