Variant (rsID / SNP)
rs6671527
rs6671527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MOB3C. Location: chromosome 1, position 47,080,679. The table records no clinical significance for this variant.
Reference-table entries
MOB3CNot classified
- Variant type
- 5_prime_UTR_premature_start_codon_gain_variant
- Chromosome / position
- 1:47080679
- HGVS
- NM_145279.5,c.-87C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.