Variant (rsID / SNP)

rs61756766

rs61756766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF13C. Location: chromosome 22, position 42,321,451. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNFRSF13CConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 22:42321451
Cytoband: 22q13.2
HGVS: NM_052945.4(TNFRSF13C):c.475C>T (p.His159Tyr)
Allele change: Missense_H159Y

Associated conditions / phenotypes

Immunodeficiency, common variable, 4

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.