Variant (rsID / SNP)
rs209373
rs209373 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRK. Location: chromosome X, position 105,152,282. The table records no clinical significance for this variant.
Reference-table entries
NRKNot classified
- Variant type
- missense_variant
- Chromosome / position
- X:105152282
- HGVS
- NM_198465.4,c.1072G>A,p.Val358Met
- Allele change
- Missense_V358M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.