Variant (rsID / SNP)
rs2907
rs2907 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP3K8. Location: chromosome 10, position 30,728,250. The table records no clinical significance for this variant.
Reference-table entries
MAP3K8Not classified
- Variant type
- intron_variant
- Chromosome / position
- 10:30728250
- HGVS
- NM_001244134.1,c.336+47A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.