Variant (rsID / SNP)
rs1126670
rs1126670 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH4. Location: chromosome 4, position 100,052,733. The table records no clinical significance for this variant.
Reference-table entries
ADH4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:100052733
- HGVS
- NM_001306171.2,c.822G>T,p.Pro274Pro
- Allele change
- Silent
Associated conditions / phenotypes
Fabry Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.