Variant (rsID / SNP)
rs3803800
rs3803800 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFSF12-TNFSF13, TNFSF13. Location: chromosome 17, position 7,462,969. The table records no clinical significance for this variant.
Reference-table entries
TNFSF12-TNFSF13Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:7462969
- HGVS
- NM_172089.4,c.527A>G,p.Asn176Ser
- Allele change
- Missense_N176S
Associated conditions / phenotypes
Iga Glomerulonephritis|Immunoglobulin Alpha Deficiency|Systemic Lupus Erythematosus|Lupus Erythematosus|Glomerulonephritis|Proteinuria, Chronic Benign|Autoimmune Disease|Leukemia, Chronic Lymphocytic|End Stage Renal Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.