Variant (rsID / SNP)
rs1949972
rs1949972 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEMA3C. Location: chromosome 7, position 80,374,438. The table records no clinical significance for this variant.
Reference-table entries
SEMA3CNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:80374438
- HGVS
- NM_001350120.2,c.2082A>G,p.Pro694Pro
- Allele change
- Synonymous_P618P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.