Variant (rsID / SNP)
rs7953704
rs7953704 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLXIP. Location: chromosome 12, position 122,625,992. The table records no clinical significance for this variant.
Reference-table entries
MLXIPNot classified
- Variant type
- intron_variant
- Chromosome / position
- 12:122625992
- HGVS
- NM_014938.6,c.2639-246A>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.