Variant (rsID / SNP)
rs4434123
rs4434123 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC9C1. Location: chromosome 3, position 111,923,123. The table records no clinical significance for this variant.
Reference-table entries
SLC9C1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:111923123
- HGVS
- NM_183061.3,c.2114C>T,p.Thr705Ile
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.