Variant (rsID / SNP)
rs13044759
rs13044759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NINL. Location: chromosome 20, position 25,484,623. The table records no clinical significance for this variant.
Reference-table entries
NINLNot classified
- Variant type
- missense_variant
- Chromosome / position
- 20:25484623
- HGVS
- NM_025176.6,c.826C>T,p.Arg276Trp
- Allele change
- Missense_R276W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.