Variant (rsID / SNP)
rs3826537
rs3826537 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRC2. Location: chromosome 17, position 60,769,803. The table records no clinical significance for this variant.
Reference-table entries
MRC2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:60769803
- HGVS
- NM_006039.5,c.4431A>G,p.Gln1477Gln
- Allele change
- Synonymous_Q1477Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.