Variant (rsID / SNP)

rs6679793

rs6679793 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCRL5. Location: chromosome 1, position 157,514,097. The table records no clinical significance for this variant.

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Reference-table entries

FCRL5Not classified

Variant type: missense_variant
Chromosome / position: 1:157514097
HGVS: NM_001195388.2,c.799T>C,p.Tyr267His
Allele change: Missense_Y267H

Associated conditions / phenotypes

Autoimmune Disease|Multiple Sclerosis|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity

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.