Variant (rsID / SNP)
rs7804122
rs7804122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEMA3A. Location: chromosome 7, position 83,634,713. The table records no clinical significance for this variant.
Reference-table entries
SEMA3ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:83634713
- HGVS
- NM_006080.3,c.1302T>C,p.Ile434Ile
- Allele change
- Synonymous_I434I
Associated conditions / phenotypes
Hirschsprung Disease 1|Exanthem|Systemic Lupus Erythematosus|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.