Variant (rsID / SNP)
rs1043879
rs1043879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RSRP1. Location: chromosome 1, position 25,570,081. The table records no clinical significance for this variant.
Reference-table entries
RSRP1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:25570081
- HGVS
- NM_001321772.2,c.716A>G,p.Glu239Gly
- Allele change
- Silent
Associated conditions / phenotypes
Rheumatoid Arthritis|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.