Variant (rsID / SNP)
rs35097172
rs35097172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A47. Location: chromosome 14, position 100,792,126. The table records no clinical significance for this variant.
Reference-table entries
SLC25A47Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 14:100792126
- HGVS
- NM_207117.4,c.30C>T,p.Gly10Gly
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.