Variant (rsID / SNP)

rs55916807

rs55916807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF13B. Location: chromosome 17, position 16,852,282. Clinical significance in the table: Likely benign.

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Reference-table entries

TNFRSF13BLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:16852282
Cytoband: 17p11.2
HGVS: NM_012452.3(TNFRSF13B):c.215G>A (p.Arg72His)
Allele change: Missense_R72H

Associated conditions / phenotypes

Common Variable Immune Deficiency, Dominant|Immunodeficiency, common variable, 2

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.