Variant (rsID / SNP)
rs1128427
rs1128427 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAEA. Location: chromosome 4, position 1,330,759. The table records no clinical significance for this variant.
Reference-table entries
MAEANot classified
- Variant type
- missense_variant
- Chromosome / position
- 4:1330759
- HGVS
- NM_001297431.2,c.676T>C,p.Trp226Arg
- Allele change
- Synonymous_A224A
Associated conditions / phenotypes
Synonymous_A291A|Synonymous_A244A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
