Variant (rsID / SNP)

rs11568821

rs11568821 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDCD1. Location: chromosome 2, position 242,793,912. Clinical significance in the table: risk factor.

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Reference-table entries

PDCD1Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 2:242793912
Cytoband: 2q37.3
HGVS: NM_005018.3(PDCD1):c.627+189G>C
Allele change: Silent

Associated conditions / phenotypes

Systemic lupus erythematosus, association wit 2|Multiple sclerosis modifier of disease progression

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.