Variant (rsID / SNP)
rs35978636
rs35978636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BANK1. Location: chromosome 4, position 102,751,014. Clinical significance in the table: Benign.
Reference-table entries
BANK1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:102751014
- Cytoband
- 4q24
- HGVS
- NM_017935.5(BANK1):c.120G>C (p.Trp40Cys)
- Allele change
- Missense_W40C
Associated conditions / phenotypes
Systemic lupus erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.