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Variant (rsID / SNP)

rs104895271

TNFRSF1A

rs104895271 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF1A. Location: chromosome 12, position 6,443,327. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNFRSF1AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:6443327
Cytoband
12p13.31
HGVS
NM_001065.4(TNFRSF1A):c.123T>G (p.Asp41Glu)
Allele change
Silent

Associated conditions / phenotypes

TNF receptor-associated periodic fever syndrome (TRAPS)|Inborn genetic diseases|Autoinflammatory syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.