Variant (rsID / SNP)

rs2234167

rs2234167 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF14. Location: chromosome 1, position 2,494,330. The table records no clinical significance for this variant.

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Reference-table entries

TNFRSF14Not classified

Variant type: single nucleotide variant
Chromosome / position: 1:2494330
Cytoband: 1p36.32
HGVS: NM_003820.4(TNFRSF14):c.721G>A (p.Val241Ile)
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.