Variant (rsID / SNP)

rs74811083

rs74811083 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF13B. Location: chromosome 17, position 16,843,708. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TNFRSF13BBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:16843708
Cytoband: 17p11.2
HGVS: NM_012452.3(TNFRSF13B):c.563A>T (p.Lys188Met)
Allele change: Missense_K188M

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.