Variant (rsID / SNP)
rs3747874
rs3747874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDFY4. Location: chromosome 10, position 50,038,800. The table records no clinical significance for this variant.
Reference-table entries
WDFY4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:50038800
- HGVS
- NM_001394531.1,c.6396A>G,p.Gln2132Gln
- Allele change
- Synonymous_Q2132Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.