Variant (rsID / SNP)
rs1132553
rs1132553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SFRP4. Location: chromosome 7, position 37,951,726. The table records no clinical significance for this variant.
Reference-table entries
SFRP4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:37951726
- HGVS
- NM_003014.4,c.786C>T,p.Arg262Arg
- Allele change
- Synonymous_R262R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.