Variant (rsID / SNP)
rs34688574
rs34688574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEURL4. Location: chromosome 17, position 7,220,881. The table records no clinical significance for this variant.
Reference-table entries
NEURL4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:7220881
- HGVS
- NM_032442.3,c.4217G>A,p.Arg1406His
- Allele change
- Missense_R1406H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
