Variant (rsID / SNP)

rs767455

rs767455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF1A. Location: chromosome 12, position 6,450,945. Clinical significance in the table: Benign.

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Reference-table entries

TNFRSF1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:6450945
Cytoband: 12p13.31
HGVS: NM_001065.4(TNFRSF1A):c.36A>G (p.Pro12=)
Allele change: Silent

Associated conditions / phenotypes

TNF receptor-associated periodic fever syndrome (TRAPS)|Susceptibility to severe coronavirus disease (COVID-19)|Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR7

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.