Variant (rsID / SNP)
rs7097397
rs7097397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDFY4. Location: chromosome 10, position 50,025,396. The table records no clinical significance for this variant.
Reference-table entries
WDFY4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:50025396
- HGVS
- NM_001394531.1,c.5447G>A,p.Arg1816Gln
- Allele change
- Missense_R1816Q
Associated conditions / phenotypes
Rheumatoid Arthritis|Systemic Lupus Erythematosus|Autoimmune Disease|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.