Variant (rsID / SNP)

rs10516487

rs10516487 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BANK1. Location: chromosome 4, position 102,751,076. Clinical significance in the table: Uncertain significance.

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Reference-table entries

BANK1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:102751076
Cytoband: 4q24
HGVS: NM_017935.5(BANK1):c.182G>A (p.Arg61His)
Allele change: Missense_R61H

Associated conditions / phenotypes

Association with systemic lupus erythematosus

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.