Variant (rsID / SNP)
rs6090471
rs6090471 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GMEB2. Location: chromosome 20, position 62,236,148. The table records no clinical significance for this variant.
Reference-table entries
GMEB2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:62236148
- HGVS
- NM_012384.5,c.177A>G,p.Ala59Ala
- Allele change
- Synonymous_A59A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.